Canonical Allele Identifier: CA2692330661
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257668_133257685dup , CM000671.2:g.133257668_133257685dup GRCh38
NC_000009.11:g.136133055_136133072dup , CM000671.1:g.136133055_136133072dup GRCh37
NC_000009.10:g.135122876_135122893dup NCBI36
NG_006669.1:g.19989_20006dup
NG_006669.2:g.22537_22554dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-136_270-119dup
ENST00000647353.1:n.54-6526_54-6509dup
ENST00000651471.1:n.329+364_329+381dup
ENST00000679909.1:c.28+17484_28+17501dup ENSP00000506089.1:n.28+17484_28+17501dup
ENST00000453660.3:n.252-136_252-119dup
ENST00000538324.2:c.240-136_240-119dup ENSP00000483018.1:n.240-136_240-119dup
ENST00000611156.4:c.240-136_240-119dup ENSP00000483265.1:n.240-136_240-119dup
NM_020469.2:c.240-136_240-119dup NP_065202.2:n.240-136_240-119dup
NM_020469.3:c.240-136_240-119dup NP_065202.2:n.240-136_240-119dup