Canonical Allele Identifier: CA1949571629
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227110C= , CM000673.2:g.5227110C= GRCh38
NC_000011.9:g.5248340C= , CM000673.1:g.5248340C= GRCh37
NC_000011.8:g.5204916C= NCBI36
NG_000007.3:g.70506G=
NG_059281.1:g.4962G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.-89G= ENSP00000494175.1:n.-89G=
ENST00000380315.2:c.-18-71G= ENSP00000369671.2:n.-18-71G=