Canonical Allele Identifier: CA467782095
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133255623-G-T
MyVariant Identifiers: chr9:g.136131010G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255623G>T , CM000671.2:g.133255623G>T GRCh38
NC_000009.11:g.136131010G>T , CM000671.1:g.136131010G>T GRCh37
NC_000009.10:g.135120831G>T NCBI36
NG_006669.1:g.22045C>A
NG_006669.2:g.24593C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1137C>A
ENST00000647353.1:n.54-4471C>A
ENST00000679909.1:c.28+19539C>A ENSP00000506089.1:n.28+19539C>A
ENST00000453660.3:n.1119C>A
ENST00000538324.2:c.1101C>A ENSP00000483018.1:p.Ser367=
ENST00000611156.4:c.*43C>A ENSP00000483265.1:n.*43C>A
NM_020469.2:c.*43C>A NP_065202.2:n.*43C>A
NM_020469.3:c.*43C>A NP_065202.2:n.*43C>A
Search 100 bp 5'
Search 100 bp 3'