Canonical Allele Identifier: CA467783711
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136132914G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257527G>C , CM000671.2:g.133257527G>C GRCh38
NC_000009.11:g.136132914G>C , CM000671.1:g.136132914G>C GRCh37
NC_000009.10:g.135122735G>C NCBI36
NG_006669.1:g.20140C>G
NG_006669.2:g.22688C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.285C>G
ENST00000647353.1:n.54-6375C>G
ENST00000651471.1:n.329+515C>G
ENST00000679909.1:c.28+17635C>G ENSP00000506089.1:n.28+17635C>G
ENST00000453660.3:n.267C>G
ENST00000538324.2:c.255C>G ENSP00000483018.1:p.Leu85=
ENST00000611156.4:c.255C>G ENSP00000483265.1:p.Leu85=
NM_020469.2:c.255C>G NP_065202.2:p.Leu85=
NM_020469.3:c.255C>G NP_065202.2:p.Leu85=