Canonical Allele Identifier: CA1949571922
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227223T= , CM000673.2:g.5227223T= GRCh38
NC_000011.9:g.5248453T= , CM000673.1:g.5248453T= GRCh37
NC_000011.8:g.5205029T= NCBI36
NG_000007.3:g.70393A=
NG_059281.1:g.4849A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380315.2:c.-18-184A= ENSP00000369671.2:n.-18-184A=