Canonical Allele Identifier: CA2579497363

Gene: ABO

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257311C>T , CM000671.2:g.133257311C>T	GRCh38
NC_000009.11:g.136132698C>T , CM000671.1:g.136132698C>T	GRCh37
NC_000009.10:g.135122519C>T	NCBI36
NG_006669.1:g.20357G>A
NG_006669.2:g.22905G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.403+98G>A
ENST00000647353.1:n.54-6159G>A
ENST00000651471.1:n.329+731G>A
ENST00000679909.1:c.28+17851G>A	ENSP00000506089.1:n.28+17851G>A
ENST00000453660.3:n.385+98G>A
ENST00000538324.2:c.371+98G>A	ENSP00000483018.1:n.371+98G>A
ENST00000611156.4:c.371+98G>A	ENSP00000483265.1:n.371+98G>A
NM_020469.2:c.374+98G>A	NP_065202.2:n.374+98G>A
NM_020469.3:c.374+98G>A	NP_065202.2:n.374+98G>A