Canonical Allele Identifier: CA467780126

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130731G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255344G>C , CM000671.2:g.133255344G>C	GRCh38
NC_000009.11:g.136130731G>C , CM000671.1:g.136130731G>C	GRCh37
NC_000009.10:g.135120552G>C	NCBI36
NG_006669.1:g.22324C>G
NG_006669.2:g.24872C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1416C>G
ENST00000647353.1:n.54-4192C>G
ENST00000679909.1:c.28+19818C>G	ENSP00000506089.1:n.28+19818C>G
ENST00000453660.3:n.1398C>G
ENST00000611156.4:c.*322C>G	ENSP00000483265.1:n.*322C>G
NM_020469.2:c.*322C>G	NP_065202.2:n.*322C>G
NM_020469.3:c.*322C>G	NP_065202.2:n.*322C>G