Canonical Allele Identifier: CA591309679

Gene: ABO

Linked Data

• dbSNP Id: rs1435644555
• gnomAD v2: 9-136135535-ACGTCGAAG-A
• MyVariant Identifiers: chr9:g.136135536_136135543del (hg19) ; chr9:g.133260132_133260139del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260133_133260140del , CM000671.2:g.133260133_133260140del	GRCh38
NC_000009.11:g.136135537_136135544del , CM000671.1:g.136135537_136135544del	GRCh37
NC_000009.10:g.135125358_135125365del	NCBI36
NG_006669.1:g.17511_17518del
NG_006669.2:g.20076_20083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.186-273_186-266del
ENST00000647353.1:n.54-8987_54-8980del
ENST00000651471.1:n.191-273_191-266del
ENST00000679909.1:c.28+15023_28+15030del	ENSP00000506089.1:n.28+15023_28+15030del
ENST00000453660.3:n.168-273_168-266del
ENST00000538324.2:c.156-273_156-266del	ENSP00000483018.1:n.156-273_156-266del
ENST00000611156.4:c.156-273_156-266del	ENSP00000483265.1:n.156-273_156-266del
NM_020469.2:c.156-273_156-266del	NP_065202.2:n.156-273_156-266del
NM_020469.3:c.156-273_156-266del	NP_065202.2:n.156-273_156-266del