Canonical Allele Identifier: CA860756213

Gene: ABO

Linked Data

• dbSNP Id: rs1167192498
• MyVariant Identifiers: chr9:g.133260302_133260303insTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133260305_133260306dup , CM000671.2:g.133260305_133260306dup	GRCh38
NC_000009.11:g.136135708_136135709dup , CM000671.1:g.136135708_136135709dup	GRCh37
NC_000009.10:g.135125529_135125530dup	NCBI36
NG_006669.1:g.17346_17347dup
NG_006669.2:g.19911_19912dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.186-438_186-437dup
ENST00000647353.1:n.54-9152_54-9151dup
ENST00000651471.1:n.191-438_191-437dup
ENST00000679909.1:c.28+14858_28+14859dup	ENSP00000506089.1:n.28+14858_28+14859dup
ENST00000453660.3:n.168-438_168-437dup
ENST00000538324.2:c.156-438_156-437dup	ENSP00000483018.1:n.156-438_156-437dup
ENST00000611156.4:c.156-438_156-437dup	ENSP00000483265.1:n.156-438_156-437dup
NM_020469.2:c.156-438_156-437dup	NP_065202.2:n.156-438_156-437dup
NM_020469.3:c.156-438_156-437dup	NP_065202.2:n.156-438_156-437dup