Canonical Allele Identifier: CA14405864

Gene: ABCC3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50636207T>G , CM000679.2:g.50636207T>G	GRCh38
NC_000017.10:g.48713568T>G , CM000679.1:g.48713568T>G	GRCh37
NC_000017.9:g.46068567T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285238.13:c.45+1226T>G MANE Select	ENSP00000285238.8:n.45+1226T>G
ENST00000285238.12:c.45+1226T>G	ENSP00000285238.8:n.45+1226T>G
ENST00000427699.5:c.45+1226T>G	ENSP00000395160.1:n.45+1226T>G
ENST00000502426.5:c.45+1226T>G	ENSP00000427073.1:n.45+1226T>G
ENST00000505699.5:c.45+1226T>G	ENSP00000427521.1:n.45+1226T>G
ENST00000513511.5:c.45+1226T>G	ENSP00000425697.1:n.45+1226T>G
NM_001144070.1:c.45+1226T>G	NP_001137542.1:n.45+1226T>G
NM_003786.3:c.45+1226T>G	NP_003777.2:n.45+1226T>G
XM_005257763.2:c.45+1226T>G	XP_005257820.1:n.45+1226T>G
XM_011525422.1:c.45+1226T>G	XP_011523724.1:n.45+1226T>G
XM_011525423.1:c.45+1226T>G	XP_011523725.1:n.45+1226T>G
XR_934586.1:n.138+1226T>G
XM_005257763.3:c.45+1226T>G	XP_005257820.1:n.45+1226T>G
XM_011525422.2:c.45+1226T>G	XP_011523724.1:n.45+1226T>G
XM_017025265.2:c.-1848+1226T>G	XP_016880754.1:n.-1848+1226T>G
XM_017025266.1:c.45+1226T>G	XP_016880755.1:n.45+1226T>G
XR_001752674.1:n.139+1226T>G
XR_934586.3:n.139+1226T>G
NM_003786.4:c.45+1226T>G MANE Select	NP_003777.2:n.45+1226T>G
NM_001144070.2:c.45+1226T>G	NP_001137542.1:n.45+1226T>G