Canonical Allele Identifier: CA2692330368

Gene: ABO

Linked Data

• gnomAD v4: 9-133256373-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256373_133256374insT , CM000671.2:g.133256373_133256374insT	GRCh38
NC_000009.11:g.136131760_136131761insT , CM000671.1:g.136131760_136131761insT	GRCh37
NC_000009.10:g.135121581_135121582insT	NCBI36
NG_006669.1:g.21294_21295insA
NG_006669.2:g.23842_23843insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404-18_404-17insA
ENST00000647353.1:n.54-5222_54-5221insA
ENST00000651471.1:n.330-18_330-17insA
ENST00000679909.1:c.28+18788_28+18789insA	ENSP00000506089.1:n.28+18788_28+18789insA
ENST00000453660.3:n.386-18_386-17insA
ENST00000538324.2:c.372-18_372-17insA	ENSP00000483018.1:n.372-18_372-17insA
ENST00000611156.4:c.372-18_372-17insA	ENSP00000483265.1:n.372-18_372-17insA
NM_020469.2:c.375-18_375-17insA	NP_065202.2:n.375-18_375-17insA
NM_020469.3:c.375-18_375-17insA	NP_065202.2:n.375-18_375-17insA