Canonical Allele Identifier: CA375686432

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131709C>G (hg19) ; chr9:g.133256322C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256322C>G , CM000671.2:g.133256322C>G	GRCh38
NC_000009.11:g.136131709C>G , CM000671.1:g.136131709C>G	GRCh37
NC_000009.10:g.135121530C>G	NCBI36
NG_006669.1:g.21346G>C
NG_006669.2:g.23894G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.438G>C
ENST00000647353.1:n.54-5170G>C
ENST00000651471.1:n.364G>C
ENST00000679909.1:c.28+18840G>C	ENSP00000506089.1:n.28+18840G>C
ENST00000453660.3:n.420G>C
ENST00000538324.2:c.406G>C	ENSP00000483018.1:p.Ala136Pro
ENST00000611156.4:c.406G>C	ENSP00000483265.1:p.Ala136Pro
NM_020469.2:c.409G>C	NP_065202.2:p.Ala137Pro
NM_020469.3:c.409G>C	NP_065202.2:p.Ala137Pro