Canonical Allele Identifier: CA860755063

Gene: ABO

Linked Data

• dbSNP Id: rs1263211900
• gnomAD v3: 9-133257826-A-ACCCC
• gnomAD v4: 9-133257826-A-ACCCC
• MyVariant Identifiers: chr9:g.136133213_136133214insCCCC (hg19) ; chr9:g.133257826_133257827insCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257828_133257831dup , CM000671.2:g.133257828_133257831dup	GRCh38
NC_000009.11:g.136133215_136133218dup , CM000671.1:g.136133215_136133218dup	GRCh37
NC_000009.10:g.135123036_135123039dup	NCBI36
NG_006669.1:g.19837_19840dup
NG_006669.2:g.22385_22388dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+267_269+270dup
ENST00000647353.1:n.54-6678_54-6675dup
ENST00000651471.1:n.329+212_329+215dup
ENST00000679909.1:c.28+17332_28+17335dup	ENSP00000506089.1:n.28+17332_28+17335dup
ENST00000453660.3:n.251+267_251+270dup
ENST00000538324.2:c.239+267_239+270dup	ENSP00000483018.1:n.239+267_239+270dup
ENST00000611156.4:c.239+267_239+270dup	ENSP00000483265.1:n.239+267_239+270dup
NM_020469.2:c.239+267_239+270dup	NP_065202.2:n.239+267_239+270dup
NM_020469.3:c.239+267_239+270dup	NP_065202.2:n.239+267_239+270dup