Canonical Allele Identifier: CA346670202

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102288C>G (hg19) ; chr2:g.43875149C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875149C>G , CM000664.2:g.43875149C>G	GRCh38
NC_000002.11:g.44102288C>G , CM000664.1:g.44102288C>G	GRCh37
NC_000002.10:g.43955792C>G	NCBI36
NG_008884.1:g.41186C>G
NG_008884.2:g.48208C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1492C>G MANE Select	ENSP00000272286.2:p.Leu498Val
ENST00000272286.2:c.1492C>G	ENSP00000272286.2:p.Leu498Val
NM_022437.2:c.1492C>G	NP_071882.1:p.Leu498Val
XM_005264483.2:c.1489C>G	XP_005264540.1:p.Leu497Val
XM_011533029.1:c.1504C>G	XP_011531331.1:p.Leu502Val
XM_011533030.1:c.1501C>G	XP_011531332.1:p.Leu501Val
XM_011533031.1:c.1276C>G	XP_011531333.1:p.Leu426Val
XR_939707.1:n.1994C>G
NM_001357321.1:c.1489C>G	NP_001344250.1:p.Leu497Val
XM_011533029.2:c.1504C>G	XP_011531331.1:p.Leu502Val
XM_011533030.2:c.1501C>G	XP_011531332.1:p.Leu501Val
XR_001738891.1:n.2008C>G
XR_939707.2:n.2008C>G
NM_022437.3:c.1492C>G MANE Select	NP_071882.1:p.Leu498Val
NM_001357321.2:c.1489C>G	NP_001344250.1:p.Leu497Val