Canonical Allele Identifier: CA346670620

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43875359-A-C
• MyVariant Identifiers: chr2:g.44102498A>C (hg19) ; chr2:g.43875359A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875359A>C , CM000664.2:g.43875359A>C	GRCh38
NC_000002.11:g.44102498A>C , CM000664.1:g.44102498A>C	GRCh37
NC_000002.10:g.43956002A>C	NCBI36
NG_008884.1:g.41396A>C
NG_008884.2:g.48418A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1702A>C MANE Select	ENSP00000272286.2:p.Asn568His
ENST00000272286.2:c.1702A>C	ENSP00000272286.2:p.Asn568His
NM_022437.2:c.1702A>C	NP_071882.1:p.Asn568His
XM_005264483.2:c.1699A>C	XP_005264540.1:p.Asn567His
XM_011533029.1:c.1714A>C	XP_011531331.1:p.Asn572His
XM_011533030.1:c.1711A>C	XP_011531332.1:p.Asn571His
XM_011533031.1:c.1486A>C	XP_011531333.1:p.Asn496His
XR_939707.1:n.2204A>C
NM_001357321.1:c.1699A>C	NP_001344250.1:p.Asn567His
XM_011533029.2:c.1714A>C	XP_011531331.1:p.Asn572His
XM_011533030.2:c.1711A>C	XP_011531332.1:p.Asn571His
XR_001738891.1:n.2218A>C
XR_939707.2:n.2218A>C
NM_022437.3:c.1702A>C MANE Select	NP_071882.1:p.Asn568His
NM_001357321.2:c.1699A>C	NP_001344250.1:p.Asn567His