Canonical Allele Identifier: CA346670822

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104738T>C (hg19) ; chr2:g.43877599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877599T>C , CM000664.2:g.43877599T>C	GRCh38
NC_000002.11:g.44104738T>C , CM000664.1:g.44104738T>C	GRCh37
NC_000002.10:g.43958242T>C	NCBI36
NG_008884.1:g.43636T>C
NG_008884.2:g.50658T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1795T>C MANE Select	ENSP00000272286.2:p.Cys599Arg
ENST00000272286.2:c.1795T>C	ENSP00000272286.2:p.Cys599Arg
NM_022437.2:c.1795T>C	NP_071882.1:p.Cys599Arg
XM_005264483.2:c.1792T>C	XP_005264540.1:p.Cys598Arg
XM_011533029.1:c.1807T>C	XP_011531331.1:p.Cys603Arg
XM_011533030.1:c.1804T>C	XP_011531332.1:p.Cys602Arg
XM_011533031.1:c.1579T>C	XP_011531333.1:p.Cys527Arg
XR_939707.1:n.2297T>C
NM_001357321.1:c.1792T>C	NP_001344250.1:p.Cys598Arg
XM_011533029.2:c.1807T>C	XP_011531331.1:p.Cys603Arg
XM_011533030.2:c.1804T>C	XP_011531332.1:p.Cys602Arg
XR_001738891.1:n.2311T>C
XR_939707.2:n.2311T>C
NM_022437.3:c.1795T>C MANE Select	NP_071882.1:p.Cys599Arg
NM_001357321.2:c.1792T>C	NP_001344250.1:p.Cys598Arg