Canonical Allele Identifier: CA375686916

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.133258198del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258198del , CM000671.2:g.133258198del	GRCh38
NC_000009.11:g.136133589del , CM000671.1:g.136133589del	GRCh37
NC_000009.10:g.135123410del	NCBI36
NG_006669.1:g.19465del
NG_006669.2:g.22017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-66del
ENST00000647353.1:n.54-7046del
ENST00000651471.1:n.239-66del
ENST00000679909.1:c.28+16964del	ENSP00000506089.1:n.28+16964del
ENST00000453660.3:n.216-66del
ENST00000538324.2:c.204-66del	ENSP00000483018.1:n.204-66del
ENST00000611156.4:c.204-66del	ENSP00000483265.1:n.204-66del
NM_020469.2:c.204-66del	NP_065202.2:n.204-66del
NM_020469.3:c.204-66del	NP_065202.2:n.204-66del