Canonical Allele Identifier: CA769063128

Gene: ABCG8

Linked Data

• dbSNP Id: rs1328125894
• MyVariant Identifiers: chr2:g.44073699A>G (hg19) ; chr2:g.43846560A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846560A>G , CM000664.2:g.43846560A>G	GRCh38
NC_000002.11:g.44073699A>G , CM000664.1:g.44073699A>G	GRCh37
NC_000002.10:g.43927203A>G	NCBI36
NG_008884.1:g.12597A>G
NG_008884.2:g.19619A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.322+249A>G MANE Select	ENSP00000272286.2:n.322+249A>G
ENST00000643284.1:n.1028A>G
ENST00000644611.1:c.334+249A>G	ENSP00000495423.1:n.334+249A>G
ENST00000272286.2:c.322+249A>G	ENSP00000272286.2:n.322+249A>G
NM_022437.2:c.322+249A>G	NP_071882.1:n.322+249A>G
XM_005264483.2:c.322+249A>G	XP_005264540.1:n.322+249A>G
XM_011533029.1:c.334+249A>G	XP_011531331.1:n.334+249A>G
XM_011533030.1:c.334+249A>G	XP_011531332.1:n.334+249A>G
XM_011533031.1:c.106+249A>G	XP_011531333.1:n.106+249A>G
XR_939707.1:n.824+249A>G
NM_001357321.1:c.322+249A>G	NP_001344250.1:n.322+249A>G
XM_011533029.2:c.334+249A>G	XP_011531331.1:n.334+249A>G
XM_011533030.2:c.334+249A>G	XP_011531332.1:n.334+249A>G
XR_001738891.1:n.838+249A>G
XR_939707.2:n.838+249A>G
NM_022437.3:c.322+249A>G MANE Select	NP_071882.1:n.322+249A>G
NM_001357321.2:c.322+249A>G	NP_001344250.1:n.322+249A>G