Canonical Allele Identifier: CA346670952

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104795G>T (hg19) ; chr2:g.43877656G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877656G>T , CM000664.2:g.43877656G>T	GRCh38
NC_000002.11:g.44104795G>T , CM000664.1:g.44104795G>T	GRCh37
NC_000002.10:g.43958299G>T	NCBI36
NG_008884.1:g.43693G>T
NG_008884.2:g.50715G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1852G>T MANE Select	ENSP00000272286.2:p.Gly618Trp
ENST00000272286.2:c.1852G>T	ENSP00000272286.2:p.Gly618Trp
NM_022437.2:c.1852G>T	NP_071882.1:p.Gly618Trp
XM_005264483.2:c.1849G>T	XP_005264540.1:p.Gly617Trp
XM_011533029.1:c.1864G>T	XP_011531331.1:p.Gly622Trp
XM_011533030.1:c.1861G>T	XP_011531332.1:p.Gly621Trp
XM_011533031.1:c.1636G>T	XP_011531333.1:p.Gly546Trp
XR_939707.1:n.2354G>T
NM_001357321.1:c.1849G>T	NP_001344250.1:p.Gly617Trp
XM_011533029.2:c.1864G>T	XP_011531331.1:p.Gly622Trp
XM_011533030.2:c.1861G>T	XP_011531332.1:p.Gly621Trp
XR_001738891.1:n.2368G>T
XR_939707.2:n.2368G>T
NM_022437.3:c.1852G>T MANE Select	NP_071882.1:p.Gly618Trp
NM_001357321.2:c.1849G>T	NP_001344250.1:p.Gly617Trp