Canonical Allele Identifier: CA1949571766
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227157G= , CM000673.2:g.5227157G= GRCh38
NC_000011.9:g.5248387G= , CM000673.1:g.5248387G= GRCh37
NC_000011.8:g.5204963G= NCBI36
NG_000007.3:g.70459C=
NG_059281.1:g.4915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-136C= ENSP00000494175.1:n.-136C=
ENST00000380315.2:c.-18-118C= ENSP00000369671.2:n.-18-118C=