Canonical Allele Identifier: CA1949571481
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227075C= , CM000673.2:g.5227075C= GRCh38
NC_000011.9:g.5248305C= , CM000673.1:g.5248305C= GRCh37
NC_000011.8:g.5204881C= NCBI36
NG_000007.3:g.70541G=
NG_059281.1:g.4997G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-54G= ENSP00000494175.1:n.-54G=
ENST00000380315.2:c.-18-36G= ENSP00000369671.2:n.-18-36G=