Canonical Allele Identifier: CA1949571483
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227077A= , CM000673.2:g.5227077A= GRCh38
NC_000011.9:g.5248307A= , CM000673.1:g.5248307A= GRCh37
NC_000011.8:g.5204883A= NCBI36
NG_000007.3:g.70539T=
NG_059281.1:g.4995T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-56T= ENSP00000494175.1:n.-56T=
ENST00000380315.2:c.-18-38T= ENSP00000369671.2:n.-18-38T=