Canonical Allele Identifier: CA467781223
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130894G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255507G>C , CM000671.2:g.133255507G>C GRCh38
NC_000009.11:g.136130894G>C , CM000671.1:g.136130894G>C GRCh37
NC_000009.10:g.135120715G>C NCBI36
NG_006669.1:g.22161C>G
NG_006669.2:g.24709C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1253C>G
ENST00000647353.1:n.54-4355C>G
ENST00000679909.1:c.28+19655C>G ENSP00000506089.1:n.28+19655C>G
ENST00000453660.3:n.1235C>G
ENST00000611156.4:c.*159C>G ENSP00000483265.1:n.*159C>G
NM_020469.2:c.*159C>G NP_065202.2:n.*159C>G
NM_020469.3:c.*159C>G NP_065202.2:n.*159C>G