Canonical Allele Identifier: CA467780112

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130727G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255340G>C , CM000671.2:g.133255340G>C	GRCh38
NC_000009.11:g.136130727G>C , CM000671.1:g.136130727G>C	GRCh37
NC_000009.10:g.135120548G>C	NCBI36
NG_006669.1:g.22328C>G
NG_006669.2:g.24876C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1420C>G
ENST00000647353.1:n.54-4188C>G
ENST00000679909.1:c.28+19822C>G	ENSP00000506089.1:n.28+19822C>G
ENST00000453660.3:n.1402C>G
ENST00000611156.4:c.*326C>G	ENSP00000483265.1:n.*326C>G
NM_020469.2:c.*326C>G	NP_065202.2:n.*326C>G
NM_020469.3:c.*326C>G	NP_065202.2:n.*326C>G