Canonical Allele Identifier: CA467780272
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1192800686
MyVariant Identifiers: chr9:g.136130760A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255373A>C , CM000671.2:g.133255373A>C GRCh38
NC_000009.11:g.136130760A>C , CM000671.1:g.136130760A>C GRCh37
NC_000009.10:g.135120581A>C NCBI36
NG_006669.1:g.22295T>G
NG_006669.2:g.24843T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1387T>G
ENST00000647353.1:n.54-4221T>G
ENST00000679909.1:c.28+19789T>G ENSP00000506089.1:n.28+19789T>G
ENST00000453660.3:n.1369T>G
ENST00000611156.4:c.*293T>G ENSP00000483265.1:n.*293T>G
NM_020469.2:c.*293T>G NP_065202.2:n.*293T>G
NM_020469.3:c.*293T>G NP_065202.2:n.*293T>G