Canonical Allele Identifier: CA1949571804
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227167C= , CM000673.2:g.5227167C= GRCh38
NC_000011.9:g.5248397C= , CM000673.1:g.5248397C= GRCh37
NC_000011.8:g.5204973C= NCBI36
NG_000007.3:g.70449G=
NG_059281.1:g.4905G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-146G= ENSP00000494175.1:n.-146G=
ENST00000380315.2:c.-18-128G= ENSP00000369671.2:n.-18-128G=