Canonical Allele Identifier: CA2580611999

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261661G>T , CM000671.2:g.133261661G>T	GRCh38
NC_000009.11:g.136137064G>T , CM000671.1:g.136137064G>T	GRCh37
NC_000009.10:g.135126885G>T	NCBI36
NG_006669.1:g.15989C>A
NG_006669.2:g.18554C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.129-287C>A
ENST00000647353.1:n.54-10509C>A
ENST00000651471.1:n.134-287C>A
ENST00000679909.1:c.28+13501C>A	ENSP00000506089.1:n.28+13501C>A
ENST00000453660.3:n.111-287C>A
ENST00000538324.2:c.99-287C>A	ENSP00000483018.1:n.99-287C>A
ENST00000611156.4:c.99-287C>A	ENSP00000483265.1:n.99-287C>A
NM_020469.2:c.99-287C>A	NP_065202.2:n.99-287C>A
NM_020469.3:c.99-287C>A	NP_065202.2:n.99-287C>A