Canonical Allele Identifier: CA467780522
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130791G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255404G>C , CM000671.2:g.133255404G>C GRCh38
NC_000009.11:g.136130791G>C , CM000671.1:g.136130791G>C GRCh37
NC_000009.10:g.135120612G>C NCBI36
NG_006669.1:g.22264C>G
NG_006669.2:g.24812C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1356C>G
ENST00000647353.1:n.54-4252C>G
ENST00000679909.1:c.28+19758C>G ENSP00000506089.1:n.28+19758C>G
ENST00000453660.3:n.1338C>G
ENST00000611156.4:c.*262C>G ENSP00000483265.1:n.*262C>G
NM_020469.2:c.*262C>G NP_065202.2:n.*262C>G
NM_020469.3:c.*262C>G NP_065202.2:n.*262C>G