Canonical Allele Identifier: CA200764865
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs7466287
MyVariant Identifiers: chr9:g.136130751G>C (hg19) chr9:g.133255364G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255364G>C , CM000671.2:g.133255364G>C GRCh38
NC_000009.11:g.136130751G>C , CM000671.1:g.136130751G>C GRCh37
NC_000009.10:g.135120572G>C NCBI36
NG_006669.1:g.22304C>G
NG_006669.2:g.24852C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1396C>G
ENST00000647353.1:n.54-4212C>G
ENST00000679909.1:c.28+19798C>G ENSP00000506089.1:n.28+19798C>G
ENST00000453660.3:n.1378C>G
ENST00000611156.4:c.*302C>G ENSP00000483265.1:n.*302C>G
NM_020469.2:c.*302C>G NP_065202.2:n.*302C>G
NM_020469.3:c.*302C>G NP_065202.2:n.*302C>G
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