Canonical Allele Identifier: CA1882584343
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1588640758
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260059A>C , CM000671.2:g.133260059A>C GRCh38
NC_000009.11:g.136135463A>C , CM000671.1:g.136135463A>C GRCh37
NC_000009.10:g.135125284A>C NCBI36
NG_006669.1:g.17591T>G
NG_006669.2:g.20156T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-193T>G
ENST00000647353.1:n.54-8907T>G
ENST00000651471.1:n.191-193T>G
ENST00000679909.1:c.28+15103T>G ENSP00000506089.1:n.28+15103T>G
ENST00000453660.3:n.168-193T>G
ENST00000538324.2:c.156-193T>G ENSP00000483018.1:n.156-193T>G
ENST00000611156.4:c.156-193T>G ENSP00000483265.1:n.156-193T>G
NM_020469.2:c.156-193T>G NP_065202.2:n.156-193T>G
NM_020469.3:c.156-193T>G NP_065202.2:n.156-193T>G
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