Canonical Allele Identifier: CA200767285
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs188088103
gnomAD v2: 9-136135472-C-T
gnomAD v3: 9-133260068-C-T
gnomAD v4: 9-133260068-C-T
MyVariant Identifiers: chr9:g.136135472C>T (hg19) chr9:g.133260068C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260068C>T , CM000671.2:g.133260068C>T GRCh38
NC_000009.11:g.136135472C>T , CM000671.1:g.136135472C>T GRCh37
NC_000009.10:g.135125293C>T NCBI36
NG_006669.1:g.17582G>A
NG_006669.2:g.20147G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-202G>A
ENST00000647353.1:n.54-8916G>A
ENST00000651471.1:n.191-202G>A
ENST00000679909.1:c.28+15094G>A ENSP00000506089.1:n.28+15094G>A
ENST00000453660.3:n.168-202G>A
ENST00000538324.2:c.156-202G>A ENSP00000483018.1:n.156-202G>A
ENST00000611156.4:c.156-202G>A ENSP00000483265.1:n.156-202G>A
NM_020469.2:c.156-202G>A NP_065202.2:n.156-202G>A
NM_020469.3:c.156-202G>A NP_065202.2:n.156-202G>A
Search 100 bp 5'
Search 100 bp 3'