Canonical Allele Identifier: CA2692330812

Gene: ABO

Linked Data

• gnomAD v4: 9-133258136-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258136C>T , CM000671.2:g.133258136C>T	GRCh38
NC_000009.11:g.136133526C>T , CM000671.1:g.136133526C>T	GRCh37
NC_000009.10:g.135123347C>T	NCBI36
NG_006669.1:g.19528G>A
NG_006669.2:g.22079G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-4G>A
ENST00000647353.1:n.54-6984G>A
ENST00000651471.1:n.239-4G>A
ENST00000679909.1:c.28+17026G>A	ENSP00000506089.1:n.28+17026G>A
ENST00000453660.3:n.216-4G>A
ENST00000538324.2:c.204-4G>A	ENSP00000483018.1:n.204-4G>A
ENST00000611156.4:c.204-4G>A	ENSP00000483265.1:n.204-4G>A
NM_020469.2:c.204-4G>A	NP_065202.2:n.204-4G>A
NM_020469.3:c.204-4G>A	NP_065202.2:n.204-4G>A