Canonical Allele Identifier: CA467853006

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131238_136131255del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255860_133255877del , CM000671.2:g.133255860_133255877del	GRCh38
NC_000009.11:g.136131247_136131264del , CM000671.1:g.136131247_136131264del	GRCh37
NC_000009.10:g.135121068_135121085del	NCBI36
NG_006669.1:g.21800_21817del
NG_006669.2:g.24348_24365del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.892_909del
ENST00000647353.1:n.54-4716_54-4699del
ENST00000679909.1:c.28+19294_28+19311del	ENSP00000506089.1:n.28+19294_28+19311del
ENST00000453660.3:n.874_891del
ENST00000538324.2:c.860_877del	ENSP00000483018.1:p.Met287_Ala292del
ENST00000611156.4:c.860_877del	ENSP00000483265.1:p.Met287_Ala292del
NM_020469.2:c.863_880del	NP_065202.2:p.Met288_Ala293del
NM_020469.3:c.863_880del	NP_065202.2:p.Met288_Ala293del