Canonical Allele Identifier: CA1949571722
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227146G= , CM000673.2:g.5227146G= GRCh38
NC_000011.9:g.5248376G= , CM000673.1:g.5248376G= GRCh37
NC_000011.8:g.5204952G= NCBI36
NG_000007.3:g.70470C=
NG_059281.1:g.4926C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-125C= ENSP00000494175.1:n.-125C=
ENST00000380315.2:c.-18-107C= ENSP00000369671.2:n.-18-107C=