Canonical Allele Identifier: CA2658820537

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43838995-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43838995G>A , CM000664.2:g.43838995G>A	GRCh38
NC_000002.11:g.44066134G>A , CM000664.1:g.44066134G>A	GRCh37
NC_000002.10:g.43919638G>A	NCBI36
NG_008883.1:g.4825C>T
NG_008884.1:g.5032G>A
NG_008884.2:g.12054G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.-59G>A MANE Select	ENSP00000272286.2:n.-59G>A
ENST00000643284.1:n.521-5512G>A
ENST00000644611.1:c.76-5512G>A	ENSP00000495423.1:n.76-5512G>A
ENST00000272286.2:c.-59G>A	ENSP00000272286.2:n.-59G>A
NM_022437.2:c.-59G>A	NP_071882.1:n.-59G>A
XM_005264483.2:c.-59G>A	XP_005264540.1:n.-59G>A
XM_011533029.1:c.76-5512G>A	XP_011531331.1:n.76-5512G>A
XM_011533030.1:c.76-5512G>A	XP_011531332.1:n.76-5512G>A
XM_011533031.1:c.-153-5512G>A	XP_011531333.1:n.-153-5512G>A
XR_939707.1:n.566-5512G>A
NM_001357321.1:c.-59G>A	NP_001344250.1:n.-59G>A
XM_011533029.2:c.76-5512G>A	XP_011531331.1:n.76-5512G>A
XM_011533030.2:c.76-5512G>A	XP_011531332.1:n.76-5512G>A
XR_001738891.1:n.580-5512G>A
XR_939707.2:n.580-5512G>A
NM_022437.3:c.-59G>A MANE Select	NP_071882.1:n.-59G>A
NM_001357321.2:c.-59G>A	NP_001344250.1:n.-59G>A