Canonical Allele Identifier: CA860757295
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1347292228
MyVariant Identifiers: chr9:g.133261745A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261745A>C , CM000671.2:g.133261745A>C GRCh38
NC_000009.11:g.136137148A>C , CM000671.1:g.136137148A>C GRCh37
NC_000009.10:g.135126969A>C NCBI36
NG_006669.1:g.15905T>G
NG_006669.2:g.18470T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+354T>G
ENST00000647353.1:n.54-10593T>G
ENST00000651471.1:n.133+354T>G
ENST00000679909.1:c.28+13417T>G ENSP00000506089.1:n.28+13417T>G
ENST00000453660.3:n.110+354T>G
ENST00000538324.2:c.98+354T>G ENSP00000483018.1:n.98+354T>G
ENST00000611156.4:c.98+354T>G ENSP00000483265.1:n.98+354T>G
NM_020469.2:c.98+354T>G NP_065202.2:n.98+354T>G
NM_020469.3:c.98+354T>G NP_065202.2:n.98+354T>G