Canonical Allele Identifier: CA591309510
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1425011410
gnomAD v2: 9-136133769-C-A
gnomAD v3: 9-133258378-C-A
gnomAD v4: 9-133258378-C-A
MyVariant Identifiers: chr9:g.136133769C>A (hg19) chr9:g.133258378C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258378C>A , CM000671.2:g.133258378C>A GRCh38
NC_000009.11:g.136133769C>A , CM000671.1:g.136133769C>A GRCh37
NC_000009.10:g.135123590C>A NCBI36
NG_006669.1:g.19285G>T
NG_006669.2:g.21837G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-246G>T
ENST00000647353.1:n.54-7226G>T
ENST00000651471.1:n.239-246G>T
ENST00000679909.1:c.28+16784G>T ENSP00000506089.1:n.28+16784G>T
ENST00000453660.3:n.216-246G>T
ENST00000538324.2:c.204-246G>T ENSP00000483018.1:n.204-246G>T
ENST00000611156.4:c.204-246G>T ENSP00000483265.1:n.204-246G>T
NM_020469.2:c.204-246G>T NP_065202.2:n.204-246G>T
NM_020469.3:c.204-246G>T NP_065202.2:n.204-246G>T
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