Canonical Allele Identifier: CA346670585

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102481T>A (hg19) ; chr2:g.43875342T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875342T>A , CM000664.2:g.43875342T>A	GRCh38
NC_000002.11:g.44102481T>A , CM000664.1:g.44102481T>A	GRCh37
NC_000002.10:g.43955985T>A	NCBI36
NG_008884.1:g.41379T>A
NG_008884.2:g.48401T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1685T>A MANE Select	ENSP00000272286.2:p.Phe562Tyr
ENST00000272286.2:c.1685T>A	ENSP00000272286.2:p.Phe562Tyr
NM_022437.2:c.1685T>A	NP_071882.1:p.Phe562Tyr
XM_005264483.2:c.1682T>A	XP_005264540.1:p.Phe561Tyr
XM_011533029.1:c.1697T>A	XP_011531331.1:p.Phe566Tyr
XM_011533030.1:c.1694T>A	XP_011531332.1:p.Phe565Tyr
XM_011533031.1:c.1469T>A	XP_011531333.1:p.Phe490Tyr
XR_939707.1:n.2187T>A
NM_001357321.1:c.1682T>A	NP_001344250.1:p.Phe561Tyr
XM_011533029.2:c.1697T>A	XP_011531331.1:p.Phe566Tyr
XM_011533030.2:c.1694T>A	XP_011531332.1:p.Phe565Tyr
XR_001738891.1:n.2201T>A
XR_939707.2:n.2201T>A
NM_022437.3:c.1685T>A MANE Select	NP_071882.1:p.Phe562Tyr
NM_001357321.2:c.1682T>A	NP_001344250.1:p.Phe561Tyr