Canonical Allele Identifier: CA375686537
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136132801G>C (hg19) chr9:g.133257414G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257414G>C , CM000671.2:g.133257414G>C GRCh38
NC_000009.11:g.136132801G>C , CM000671.1:g.136132801G>C GRCh37
NC_000009.10:g.135122622G>C NCBI36
NG_006669.1:g.20254C>G
NG_006669.2:g.22802C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.398C>G
ENST00000647353.1:n.54-6262C>G
ENST00000651471.1:n.329+628C>G
ENST00000679909.1:c.28+17748C>G ENSP00000506089.1:n.28+17748C>G
ENST00000453660.3:n.380C>G
ENST00000538324.2:c.366C>G ENSP00000483018.1:p.Ile122Met
ENST00000611156.4:c.366C>G ENSP00000483265.1:p.Ile122Met
NM_020469.2:c.369C>G NP_065202.2:p.Ile123Met
NM_020469.3:c.369C>G NP_065202.2:p.Ile123Met
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