Canonical Allele Identifier: CA11686017

Gene: APBB2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41000929G>C , CM000666.2:g.41000929G>C	GRCh38
NC_000004.11:g.41002946G>C , CM000666.1:g.41002946G>C	GRCh37
NC_000004.10:g.40697703G>C	NCBI36
NG_013337.1:g.218690C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508593.6:c.835+12654C>G MANE Select	ENSP00000427211.1:n.835+12654C>G
ENST00000295974.12:c.835+12654C>G	ENSP00000295974.8:n.835+12654C>G
ENST00000506352.5:c.835+12654C>G	ENSP00000421539.1:n.835+12654C>G
ENST00000508593.5:c.835+12654C>G	ENSP00000427211.1:n.835+12654C>G
ENST00000509475.5:n.803+12654C>G
ENST00000513140.5:c.835+12654C>G	ENSP00000426018.1:n.835+12654C>G
ENST00000513611.5:c.803+12654C>G
NM_001166050.1:c.835+12654C>G	NP_001159522.1:n.835+12654C>G
NM_004307.1:c.835+12654C>G	NP_004298.1:n.835+12654C>G
NM_173075.4:c.835+12654C>G	NP_775098.2:n.835+12654C>G
XM_005248101.2:c.835+12654C>G	XP_005248158.1:n.835+12654C>G
XM_006714005.2:c.835+12654C>G	XP_006714068.1:n.835+12654C>G
XM_006714006.2:c.835+12654C>G	XP_006714069.1:n.835+12654C>G
XM_006714007.2:c.835+12654C>G	XP_006714070.1:n.835+12654C>G
XM_006714008.2:c.835+12654C>G	XP_006714071.1:n.835+12654C>G
XM_006714009.2:c.835+12654C>G	XP_006714072.1:n.835+12654C>G
XM_006714010.2:c.835+12654C>G	XP_006714073.1:n.835+12654C>G
XM_006714011.2:c.835+12654C>G	XP_006714074.1:n.835+12654C>G
XM_006714012.2:c.835+12654C>G	XP_006714075.1:n.835+12654C>G
XM_011513686.1:c.835+12654C>G	XP_011511988.1:n.835+12654C>G
XM_011513687.1:c.835+12654C>G	XP_011511989.1:n.835+12654C>G
XM_011513688.1:c.835+12654C>G	XP_011511990.1:n.835+12654C>G
NM_001330656.1:c.835+12654C>G	NP_001317585.1:n.835+12654C>G
NM_001330658.1:c.835+12654C>G	NP_001317587.1:n.835+12654C>G
XM_006714005.4:c.835+12654C>G	XP_006714068.1:n.835+12654C>G
XM_006714007.4:c.835+12654C>G	XP_006714070.1:n.835+12654C>G
XM_006714008.4:c.835+12654C>G	XP_006714071.1:n.835+12654C>G
XM_006714009.4:c.835+12654C>G	XP_006714072.1:n.835+12654C>G
XM_006714010.4:c.835+12654C>G	XP_006714073.1:n.835+12654C>G
XM_006714011.4:c.835+12654C>G	XP_006714074.1:n.835+12654C>G
XM_006714012.4:c.835+12654C>G	XP_006714075.1:n.835+12654C>G
XM_011513686.3:c.835+12654C>G	XP_011511988.1:n.835+12654C>G
XM_011513687.3:c.835+12654C>G	XP_011511989.1:n.835+12654C>G
XM_011513688.3:c.835+12654C>G	XP_011511990.1:n.835+12654C>G
XM_017008143.2:c.835+12654C>G	XP_016863632.1:n.835+12654C>G
XM_017008144.2:c.835+12654C>G	XP_016863633.1:n.835+12654C>G
XM_017008145.2:c.835+12654C>G	XP_016863634.1:n.835+12654C>G
XM_017008146.2:c.784+12654C>G	XP_016863635.1:n.784+12654C>G
XM_017008147.2:c.784+12654C>G	XP_016863636.1:n.784+12654C>G
XM_017008148.2:c.784+12654C>G	XP_016863637.1:n.784+12654C>G
XM_017008149.2:c.784+12654C>G	XP_016863638.1:n.784+12654C>G
XM_017008151.2:c.835+12654C>G	XP_016863640.1:n.835+12654C>G
XM_017008152.2:c.835+12654C>G	XP_016863641.1:n.835+12654C>G
XM_017008154.2:c.835+12654C>G	XP_016863643.1:n.835+12654C>G
XM_017008156.2:c.784+12654C>G	XP_016863645.1:n.784+12654C>G
XM_017008157.2:c.784+12654C>G	XP_016863646.1:n.784+12654C>G
XM_017008158.2:c.784+12654C>G	XP_016863647.1:n.784+12654C>G
NM_004307.2:c.835+12654C>G MANE Select	NP_004298.1:n.835+12654C>G
NM_001166050.2:c.835+12654C>G	NP_001159522.1:n.835+12654C>G
NM_001330656.2:c.835+12654C>G	NP_001317585.1:n.835+12654C>G
NM_001330658.2:c.835+12654C>G	NP_001317587.1:n.835+12654C>G
NM_173075.5:c.835+12654C>G	NP_775098.2:n.835+12654C>G