Canonical Allele Identifier: CA591308936
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1251205989

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257164C>T , CM000671.2:g.133257164C>T GRCh38
NC_000009.11:g.136132551C>T , CM000671.1:g.136132551C>T GRCh37
NC_000009.10:g.135122372C>T NCBI36
NG_006669.1:g.20504G>A
NG_006669.2:g.23052G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+245G>A
ENST00000647353.1:n.54-6012G>A
ENST00000651471.1:n.330-808G>A
ENST00000679909.1:c.28+17998G>A ENSP00000506089.1:n.28+17998G>A
ENST00000453660.3:n.385+245G>A
ENST00000538324.2:c.371+245G>A ENSP00000483018.1:n.371+245G>A
ENST00000611156.4:c.371+245G>A ENSP00000483265.1:n.371+245G>A
NM_020469.2:c.374+245G>A NP_065202.2:n.374+245G>A
NM_020469.3:c.374+245G>A NP_065202.2:n.374+245G>A