Canonical Allele Identifier: CA591377488

Gene: ABO

Linked Data

• dbSNP Id: rs1276738861
• gnomAD v2: 9-136131209-CTCG-C
• gnomAD v4: 9-133255822-CTCG-C
• MyVariant Identifiers: chr9:g.136131210_136131212del (hg19) ; chr9:g.133255823_133255825del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255827_133255829del , CM000671.2:g.133255827_133255829del	GRCh38
NC_000009.11:g.136131214_136131216del , CM000671.1:g.136131214_136131216del	GRCh37
NC_000009.10:g.135121035_135121037del	NCBI36
NG_006669.1:g.21843_21845del
NG_006669.2:g.24391_24393del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.935_937del
ENST00000647353.1:n.54-4673_54-4671del
ENST00000679909.1:c.28+19337_28+19339del	ENSP00000506089.1:n.28+19337_28+19339del
ENST00000453660.3:n.917_919del
ENST00000538324.2:c.903_905del	ENSP00000483018.1:p.Asp301del
ENST00000611156.4:c.903_905del	ENSP00000483265.1:p.Asp301del
NM_020469.2:c.906_908del	NP_065202.2:p.Asp302del
NM_020469.3:c.906_908del	NP_065202.2:p.Asp302del