Canonical Allele Identifier: CA467782922

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131647G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256260G>C , CM000671.2:g.133256260G>C	GRCh38
NC_000009.11:g.136131647G>C , CM000671.1:g.136131647G>C	GRCh37
NC_000009.10:g.135121468G>C	NCBI36
NG_006669.1:g.21408C>G
NG_006669.2:g.23956C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.500C>G
ENST00000647353.1:n.54-5108C>G
ENST00000651471.1:n.426C>G
ENST00000679909.1:c.28+18902C>G	ENSP00000506089.1:n.28+18902C>G
ENST00000453660.3:n.482C>G
ENST00000538324.2:c.468C>G	ENSP00000483018.1:p.Ala156=
ENST00000611156.4:c.468C>G	ENSP00000483265.1:p.Ala156=
NM_020469.2:c.471C>G	NP_065202.2:p.Ala157=
NM_020469.3:c.471C>G	NP_065202.2:p.Ala157=