Canonical Allele Identifier: CA1949571939
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227252G= , CM000673.2:g.5227252G= GRCh38
NC_000011.9:g.5248482G= , CM000673.1:g.5248482G= GRCh37
NC_000011.8:g.5205058G= NCBI36
NG_000007.3:g.70364C=
NG_059281.1:g.4820C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380315.2:c.-18-213C= ENSP00000369671.2:n.-18-213C=