Canonical Allele Identifier: CA346670594

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43875345-G-A
• MyVariant Identifiers: chr2:g.44102484G>A (hg19) ; chr2:g.43875345G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875345G>A , CM000664.2:g.43875345G>A	GRCh38
NC_000002.11:g.44102484G>A , CM000664.1:g.44102484G>A	GRCh37
NC_000002.10:g.43955988G>A	NCBI36
NG_008884.1:g.41382G>A
NG_008884.2:g.48404G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1688G>A MANE Select	ENSP00000272286.2:p.Ser563Asn
ENST00000272286.2:c.1688G>A	ENSP00000272286.2:p.Ser563Asn
NM_022437.2:c.1688G>A	NP_071882.1:p.Ser563Asn
XM_005264483.2:c.1685G>A	XP_005264540.1:p.Ser562Asn
XM_011533029.1:c.1700G>A	XP_011531331.1:p.Ser567Asn
XM_011533030.1:c.1697G>A	XP_011531332.1:p.Ser566Asn
XM_011533031.1:c.1472G>A	XP_011531333.1:p.Ser491Asn
XR_939707.1:n.2190G>A
NM_001357321.1:c.1685G>A	NP_001344250.1:p.Ser562Asn
XM_011533029.2:c.1700G>A	XP_011531331.1:p.Ser567Asn
XM_011533030.2:c.1697G>A	XP_011531332.1:p.Ser566Asn
XR_001738891.1:n.2204G>A
XR_939707.2:n.2204G>A
NM_022437.3:c.1688G>A MANE Select	NP_071882.1:p.Ser563Asn
NM_001357321.2:c.1685G>A	NP_001344250.1:p.Ser562Asn