Canonical Allele Identifier: CA2658838226

Gene: ABCG8

Linked Data

• gnomAD v4: 2-43878081-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43878081T>A , CM000664.2:g.43878081T>A	GRCh38
NC_000002.11:g.44105220T>A , CM000664.1:g.44105220T>A	GRCh37
NC_000002.10:g.43958724T>A	NCBI36
NG_008884.1:g.44118T>A
NG_008884.2:g.51140T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.*168T>A MANE Select	ENSP00000272286.2:n.*168T>A
ENST00000272286.2:c.*168T>A	ENSP00000272286.2:n.*168T>A
NM_022437.2:c.*168T>A	NP_071882.1:n.*168T>A
XM_005264483.2:c.*168T>A	XP_005264540.1:n.*168T>A
XM_011533029.1:c.*168T>A	XP_011531331.1:n.*168T>A
XM_011533030.1:c.*168T>A	XP_011531332.1:n.*168T>A
XM_011533031.1:c.*168T>A	XP_011531333.1:n.*168T>A
XR_939707.1:n.2692T>A
NM_001357321.1:c.*168T>A	NP_001344250.1:n.*168T>A
XM_011533029.2:c.*168T>A	XP_011531331.1:n.*168T>A
XM_011533030.2:c.*168T>A	XP_011531332.1:n.*168T>A
XR_001738891.1:n.2706T>A
XR_939707.2:n.2706T>A
NM_022437.3:c.*168T>A MANE Select	NP_071882.1:n.*168T>A
NM_001357321.2:c.*168T>A	NP_001344250.1:n.*168T>A