Canonical Allele Identifier: CA1949571525
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227095A= , CM000673.2:g.5227095A= GRCh38
NC_000011.9:g.5248325A= , CM000673.1:g.5248325A= GRCh37
NC_000011.8:g.5204901A= NCBI36
NG_000007.3:g.70521T=
NG_059281.1:g.4977T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-74T= ENSP00000494175.1:n.-74T=
ENST00000380315.2:c.-18-56T= ENSP00000369671.2:n.-18-56T=