Canonical Allele Identifier: CA591309668
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1198767807
gnomAD v2: 9-136135495-C-G
gnomAD v3: 9-133260091-C-G
gnomAD v4: 9-133260091-C-G
MyVariant Identifiers: chr9:g.136135495C>G (hg19) chr9:g.133260091C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260091C>G , CM000671.2:g.133260091C>G GRCh38
NC_000009.11:g.136135495C>G , CM000671.1:g.136135495C>G GRCh37
NC_000009.10:g.135125316C>G NCBI36
NG_006669.1:g.17559G>C
NG_006669.2:g.20124G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-225G>C
ENST00000647353.1:n.54-8939G>C
ENST00000651471.1:n.191-225G>C
ENST00000679909.1:c.28+15071G>C ENSP00000506089.1:n.28+15071G>C
ENST00000453660.3:n.168-225G>C
ENST00000538324.2:c.156-225G>C ENSP00000483018.1:n.156-225G>C
ENST00000611156.4:c.156-225G>C ENSP00000483265.1:n.156-225G>C
NM_020469.2:c.156-225G>C NP_065202.2:n.156-225G>C
NM_020469.3:c.156-225G>C NP_065202.2:n.156-225G>C
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