Canonical Allele Identifier: CA2692330406

Gene: ABO

Linked Data

• gnomAD v4: 9-133256435-CCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256438_133256440del , CM000671.2:g.133256438_133256440del	GRCh38
NC_000009.11:g.136131825_136131827del , CM000671.1:g.136131825_136131827del	GRCh37
NC_000009.10:g.135121646_135121648del	NCBI36
NG_006669.1:g.21230_21232del
NG_006669.2:g.23778_23780del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404-82_404-80del
ENST00000647353.1:n.54-5286_54-5284del
ENST00000651471.1:n.330-82_330-80del
ENST00000679909.1:c.28+18724_28+18726del	ENSP00000506089.1:n.28+18724_28+18726del
ENST00000453660.3:n.386-82_386-80del
ENST00000538324.2:c.372-82_372-80del	ENSP00000483018.1:n.372-82_372-80del
ENST00000611156.4:c.372-82_372-80del	ENSP00000483265.1:n.372-82_372-80del
NM_020469.2:c.375-82_375-80del	NP_065202.2:n.375-82_375-80del
NM_020469.3:c.375-82_375-80del	NP_065202.2:n.375-82_375-80del