Canonical Allele Identifier: CA346670228

Gene: ABCG8

Linked Data

• dbSNP Id: rs761153163
• gnomAD v4: 2-43875162-C-A
• MyVariant Identifiers: chr2:g.44102301C>A (hg19) ; chr2:g.43875162C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875162C>A , CM000664.2:g.43875162C>A	GRCh38
NC_000002.11:g.44102301C>A , CM000664.1:g.44102301C>A	GRCh37
NC_000002.10:g.43955805C>A	NCBI36
NG_008884.1:g.41199C>A
NG_008884.2:g.48221C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1505C>A MANE Select	ENSP00000272286.2:p.Pro502Gln
ENST00000272286.2:c.1505C>A	ENSP00000272286.2:p.Pro502Gln
NM_022437.2:c.1505C>A	NP_071882.1:p.Pro502Gln
XM_005264483.2:c.1502C>A	XP_005264540.1:p.Pro501Gln
XM_011533029.1:c.1517C>A	XP_011531331.1:p.Pro506Gln
XM_011533030.1:c.1514C>A	XP_011531332.1:p.Pro505Gln
XM_011533031.1:c.1289C>A	XP_011531333.1:p.Pro430Gln
XR_939707.1:n.2007C>A
NM_001357321.1:c.1502C>A	NP_001344250.1:p.Pro501Gln
XM_011533029.2:c.1517C>A	XP_011531331.1:p.Pro506Gln
XM_011533030.2:c.1514C>A	XP_011531332.1:p.Pro505Gln
XR_001738891.1:n.2021C>A
XR_939707.2:n.2021C>A
NM_022437.3:c.1505C>A MANE Select	NP_071882.1:p.Pro502Gln
NM_001357321.2:c.1502C>A	NP_001344250.1:p.Pro501Gln