Canonical Allele Identifier: CA1882580499
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256158_133256159delinsCA , CM000671.2:g.133256158_133256159delinsCA GRCh38
NC_000009.11:g.136131545_136131546delinsCA , CM000671.1:g.136131545_136131546delinsCA GRCh37
NC_000009.10:g.135121366_135121367delinsCA NCBI36
NG_006669.1:g.21509_21510delinsTG
NG_006669.2:g.24057_24058delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.601_602delinsTG
ENST00000647353.1:n.54-5007_54-5006delinsTG
ENST00000651471.1:n.527_528delinsTG
ENST00000679909.1:c.28+19003_28+19004delinsTG ENSP00000506089.1:n.28+19003_28+19004delinsTG
ENST00000453660.3:n.583_584delinsTG
ENST00000538324.2:c.569_570delinsTG ENSP00000483018.1:p.Met190=
ENST00000611156.4:c.569_570delinsTG ENSP00000483265.1:p.Met190=
NM_020469.2:c.572_573delinsTG NP_065202.2:p.Met191=
NM_020469.3:c.572_573delinsTG NP_065202.2:p.Met191=