Canonical Allele Identifier: CA2579829165
Gene: HBB HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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