Canonical Allele Identifier: CA467780148
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133255351-T-G
MyVariant Identifiers: chr9:g.136130738T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255351T>G , CM000671.2:g.133255351T>G GRCh38
NC_000009.11:g.136130738T>G , CM000671.1:g.136130738T>G GRCh37
NC_000009.10:g.135120559T>G NCBI36
NG_006669.1:g.22317A>C
NG_006669.2:g.24865A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1409A>C
ENST00000647353.1:n.54-4199A>C
ENST00000679909.1:c.28+19811A>C ENSP00000506089.1:n.28+19811A>C
ENST00000453660.3:n.1391A>C
ENST00000611156.4:c.*315A>C ENSP00000483265.1:n.*315A>C
NM_020469.2:c.*315A>C NP_065202.2:n.*315A>C
NM_020469.3:c.*315A>C NP_065202.2:n.*315A>C
Search 100 bp 5'
Search 100 bp 3'