Canonical Allele Identifier: CA860757156

Gene: ABO

Linked Data

• dbSNP Id: rs139240629
• gnomAD v3: 9-133261600-G-C
• gnomAD v4: 9-133261600-G-C
• MyVariant Identifiers: chr9:g.133261600G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261600G>C , CM000671.2:g.133261600G>C	GRCh38
NC_000009.11:g.136137003G>C , CM000671.1:g.136137003G>C	GRCh37
NC_000009.10:g.135126824G>C	NCBI36
NG_006669.1:g.16050C>G
NG_006669.2:g.18615C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.129-226C>G
ENST00000647353.1:n.54-10448C>G
ENST00000651471.1:n.134-226C>G
ENST00000679909.1:c.28+13562C>G	ENSP00000506089.1:n.28+13562C>G
ENST00000453660.3:n.111-226C>G
ENST00000538324.2:c.99-226C>G	ENSP00000483018.1:n.99-226C>G
ENST00000611156.4:c.99-226C>G	ENSP00000483265.1:n.99-226C>G
NM_020469.2:c.99-226C>G	NP_065202.2:n.99-226C>G
NM_020469.3:c.99-226C>G	NP_065202.2:n.99-226C>G