Canonical Allele Identifier: CA860757204
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs687621
MyVariant Identifiers: chr9:g.133261662G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261662G>C , CM000671.2:g.133261662G>C GRCh38
NG_006669.2:g.18553C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-288C>G
ENST00000647353.1:n.54-10510C>G
ENST00000651471.1:n.134-288C>G
ENST00000679909.1:c.28+13500C>G ENSP00000506089.1:n.28+13500C>G
ENST00000453660.3:n.111-288C>G
ENST00000538324.2:c.99-288C>G ENSP00000483018.1:n.99-288C>G
ENST00000611156.4:c.99-288C>G ENSP00000483265.1:n.99-288C>G
NM_020469.2:c.99-288C>G NP_065202.2:n.99-288C>G
NM_020469.3:c.99-288C>G NP_065202.2:n.99-288C>G