Canonical Allele Identifier: CA1949571862
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227181_5227182delinsCT , CM000673.2:g.5227181_5227182delinsCT GRCh38
NC_000011.9:g.5248411_5248412delinsCT , CM000673.1:g.5248411_5248412delinsCT GRCh37
NC_000011.8:g.5204987_5204988delinsCT NCBI36
NG_000007.3:g.70434_70435delinsAG
NG_059281.1:g.4890_4891delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-161_-160delinsAG ENSP00000494175.1:n.-161_-160delinsAG
ENST00000380315.2:c.-18-143_-18-142delinsAG ENSP00000369671.2:n.-18-143_-18-142delinsAG