Canonical Allele Identifier: CA467781764

Gene: ABO

Linked Data

• dbSNP Id: rs1424449330
• gnomAD v3: 9-133255571-C-A
• gnomAD v4: 9-133255571-C-A
• MyVariant Identifiers: chr9:g.136130958C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255571C>A , CM000671.2:g.133255571C>A	GRCh38
NC_000009.11:g.136130958C>A , CM000671.1:g.136130958C>A	GRCh37
NC_000009.10:g.135120779C>A	NCBI36
NG_006669.1:g.22097G>T
NG_006669.2:g.24645G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1189G>T
ENST00000647353.1:n.54-4419G>T
ENST00000679909.1:c.28+19591G>T	ENSP00000506089.1:n.28+19591G>T
ENST00000453660.3:n.1171G>T
ENST00000611156.4:c.*95G>T	ENSP00000483265.1:n.*95G>T
NM_020469.2:c.*95G>T	NP_065202.2:n.*95G>T
NM_020469.3:c.*95G>T	NP_065202.2:n.*95G>T