Canonical Allele Identifier: CA467781294
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1309203586
MyVariant Identifiers: chr9:g.136130903G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255516G>C , CM000671.2:g.133255516G>C GRCh38
NC_000009.11:g.136130903G>C , CM000671.1:g.136130903G>C GRCh37
NC_000009.10:g.135120724G>C NCBI36
NG_006669.1:g.22152C>G
NG_006669.2:g.24700C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1244C>G
ENST00000647353.1:n.54-4364C>G
ENST00000679909.1:c.28+19646C>G ENSP00000506089.1:n.28+19646C>G
ENST00000453660.3:n.1226C>G
ENST00000611156.4:c.*150C>G ENSP00000483265.1:n.*150C>G
NM_020469.2:c.*150C>G NP_065202.2:n.*150C>G
NM_020469.3:c.*150C>G NP_065202.2:n.*150C>G