Canonical Allele Identifier: CA1949571626
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227104C= , CM000673.2:g.5227104C= GRCh38
NC_000011.9:g.5248334C= , CM000673.1:g.5248334C= GRCh37
NC_000011.8:g.5204910C= NCBI36
NG_000007.3:g.70512G=
NG_059281.1:g.4968G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-83G= ENSP00000494175.1:n.-83G=
ENST00000380315.2:c.-18-65G= ENSP00000369671.2:n.-18-65G=