Canonical Allele Identifier: CA2579829169
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227098T>C , CM000673.2:g.5227098T>C GRCh38
NC_000011.9:g.5248328T>C , CM000673.1:g.5248328T>C GRCh37
NC_000011.8:g.5204904T>C NCBI36
NG_000007.3:g.70518A>G
NG_059281.1:g.4974A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-77A>G ENSP00000494175.1:n.-77A>G
ENST00000380315.2:c.-18-59A>G ENSP00000369671.2:n.-18-59A>G