Canonical Allele Identifier: CA769063114

Gene: ABCG8

Linked Data

• dbSNP Id: rs1276967802
• gnomAD v3: 2-43846530-T-C
• gnomAD v4: 2-43846530-T-C
• MyVariant Identifiers: chr2:g.44073669T>C (hg19) ; chr2:g.43846530T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846530T>C , CM000664.2:g.43846530T>C	GRCh38
NC_000002.11:g.44073669T>C , CM000664.1:g.44073669T>C	GRCh37
NC_000002.10:g.43927173T>C	NCBI36
NG_008884.1:g.12567T>C
NG_008884.2:g.19589T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.322+219T>C MANE Select	ENSP00000272286.2:n.322+219T>C
ENST00000643284.1:n.998T>C
ENST00000644611.1:c.334+219T>C	ENSP00000495423.1:n.334+219T>C
ENST00000272286.2:c.322+219T>C	ENSP00000272286.2:n.322+219T>C
NM_022437.2:c.322+219T>C	NP_071882.1:n.322+219T>C
XM_005264483.2:c.322+219T>C	XP_005264540.1:n.322+219T>C
XM_011533029.1:c.334+219T>C	XP_011531331.1:n.334+219T>C
XM_011533030.1:c.334+219T>C	XP_011531332.1:n.334+219T>C
XM_011533031.1:c.106+219T>C	XP_011531333.1:n.106+219T>C
XR_939707.1:n.824+219T>C
NM_001357321.1:c.322+219T>C	NP_001344250.1:n.322+219T>C
XM_011533029.2:c.334+219T>C	XP_011531331.1:n.334+219T>C
XM_011533030.2:c.334+219T>C	XP_011531332.1:n.334+219T>C
XR_001738891.1:n.838+219T>C
XR_939707.2:n.838+219T>C
NM_022437.3:c.322+219T>C MANE Select	NP_071882.1:n.322+219T>C
NM_001357321.2:c.322+219T>C	NP_001344250.1:n.322+219T>C