Canonical Allele Identifier: CA860755086

Gene: ABO

Linked Data

• dbSNP Id: rs1338760928
• MyVariant Identifiers: chr9:g.136133250del (hg19) ; chr9:g.133257863del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257863del , CM000671.2:g.133257863del	GRCh38
NC_000009.11:g.136133250del , CM000671.1:g.136133250del	GRCh37
NC_000009.10:g.135123071del	NCBI36
NG_006669.1:g.19804del
NG_006669.2:g.22352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+234del
ENST00000647353.1:n.54-6711del
ENST00000651471.1:n.329+179del
ENST00000679909.1:c.28+17299del	ENSP00000506089.1:n.28+17299del
ENST00000453660.3:n.251+234del
ENST00000538324.2:c.239+234del	ENSP00000483018.1:n.239+234del
ENST00000611156.4:c.239+234del	ENSP00000483265.1:n.239+234del
NM_020469.2:c.239+234del	NP_065202.2:n.239+234del
NM_020469.3:c.239+234del	NP_065202.2:n.239+234del