Canonical Allele Identifier: CA467780327
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1754604310
MyVariant Identifiers: chr9:g.136130768T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255381T>C , CM000671.2:g.133255381T>C GRCh38
NC_000009.11:g.136130768T>C , CM000671.1:g.136130768T>C GRCh37
NC_000009.10:g.135120589T>C NCBI36
NG_006669.1:g.22287A>G
NG_006669.2:g.24835A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1379A>G
ENST00000647353.1:n.54-4229A>G
ENST00000679909.1:c.28+19781A>G ENSP00000506089.1:n.28+19781A>G
ENST00000453660.3:n.1361A>G
ENST00000611156.4:c.*285A>G ENSP00000483265.1:n.*285A>G
NM_020469.2:c.*285A>G NP_065202.2:n.*285A>G
NM_020469.3:c.*285A>G NP_065202.2:n.*285A>G