Canonical Allele Identifier: CA532703108

Gene: ABCG8

Linked Data

• dbSNP Id: rs377340438
• gnomAD v2: 2-44073455-C-A
• gnomAD v4: 2-43846316-C-A
• MyVariant Identifiers: chr2:g.44073455C>A (hg19) ; chr2:g.43846316C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846316C>A , CM000664.2:g.43846316C>A	GRCh38
NC_000002.11:g.44073455C>A , CM000664.1:g.44073455C>A	GRCh37
NC_000002.10:g.43926959C>A	NCBI36
NG_008884.1:g.12353C>A
NG_008884.2:g.19375C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.322+5C>A MANE Select	ENSP00000272286.2:n.322+5C>A
ENST00000643284.1:n.784C>A
ENST00000644611.1:c.334+5C>A	ENSP00000495423.1:n.334+5C>A
ENST00000272286.2:c.322+5C>A	ENSP00000272286.2:n.322+5C>A
NM_022437.2:c.322+5C>A	NP_071882.1:n.322+5C>A
XM_005264483.2:c.322+5C>A	XP_005264540.1:n.322+5C>A
XM_011533029.1:c.334+5C>A	XP_011531331.1:n.334+5C>A
XM_011533030.1:c.334+5C>A	XP_011531332.1:n.334+5C>A
XM_011533031.1:c.106+5C>A	XP_011531333.1:n.106+5C>A
XR_939707.1:n.824+5C>A
NM_001357321.1:c.322+5C>A	NP_001344250.1:n.322+5C>A
XM_011533029.2:c.334+5C>A	XP_011531331.1:n.334+5C>A
XM_011533030.2:c.334+5C>A	XP_011531332.1:n.334+5C>A
XR_001738891.1:n.838+5C>A
XR_939707.2:n.838+5C>A
NM_022437.3:c.322+5C>A MANE Select	NP_071882.1:n.322+5C>A
NM_001357321.2:c.322+5C>A	NP_001344250.1:n.322+5C>A