Canonical Allele Identifier: CA860757289
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1263076974
gnomAD v3: 9-133261735-AGGTGACTTCACTCTT-A
gnomAD v4: 9-133261735-AGGTGACTTCACTCTT-A
MyVariant Identifiers: chr9:g.133261736_133261750del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261739_133261753del , CM000671.2:g.133261739_133261753del GRCh38
NC_000009.11:g.136137142_136137156del , CM000671.1:g.136137142_136137156del GRCh37
NC_000009.10:g.135126963_135126977del NCBI36
NG_006669.1:g.15900_15914del
NG_006669.2:g.18465_18479del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+349_129-362del
ENST00000647353.1:n.54-10598_54-10584del
ENST00000651471.1:n.133+349_134-362del
ENST00000679909.1:c.28+13412_28+13426del ENSP00000506089.1:n.28+13412_28+13426del
ENST00000453660.3:n.110+349_111-362del
ENST00000538324.2:c.98+349_99-362del ENSP00000483018.1:n.98+349_99-362del
ENST00000611156.4:c.98+349_99-362del ENSP00000483265.1:n.98+349_99-362del
NM_020469.2:c.98+349_99-362del NP_065202.2:n.98+349_99-362del
NM_020469.3:c.98+349_99-362del NP_065202.2:n.98+349_99-362del
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