Canonical Allele Identifier: CA2692330567

Gene: ABO

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257524_133257526del , CM000671.2:g.133257524_133257526del	GRCh38
NC_000009.11:g.136132911_136132913del , CM000671.1:g.136132911_136132913del	GRCh37
NC_000009.10:g.135122732_135122734del	NCBI36
NG_006669.1:g.20143_20145del
NG_006669.2:g.22691_22693del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.288_290del
ENST00000647353.1:n.54-6372_54-6370del
ENST00000651471.1:n.329+518_329+520del
ENST00000679909.1:c.28+17638_28+17640del	ENSP00000506089.1:n.28+17638_28+17640del
ENST00000453660.3:n.270_272del
ENST00000538324.2:c.258_259-1del
ENST00000611156.4:c.258_259-1del
NM_020469.2:c.258_260del	NP_065202.2:p.Val87del
NM_020469.3:c.258_260del	NP_065202.2:p.Val87del