Canonical Allele Identifier: CA1129716411
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834641606

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258409G>C , CM000671.2:g.133258409G>C GRCh38
NC_000009.11:g.136133800G>C , CM000671.1:g.136133800G>C GRCh37
NC_000009.10:g.135123621G>C NCBI36
NG_006669.1:g.19254C>G
NG_006669.2:g.21806C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-277C>G
ENST00000647353.1:n.54-7257C>G
ENST00000651471.1:n.239-277C>G
ENST00000679909.1:c.28+16753C>G ENSP00000506089.1:n.28+16753C>G
ENST00000453660.3:n.216-277C>G
ENST00000538324.2:c.204-277C>G ENSP00000483018.1:n.204-277C>G
ENST00000611156.4:c.204-277C>G ENSP00000483265.1:n.204-277C>G
NM_020469.2:c.204-277C>G NP_065202.2:n.204-277C>G
NM_020469.3:c.204-277C>G NP_065202.2:n.204-277C>G