Canonical Allele Identifier: CA217114301
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 869345
ClinVar RCV Id: RCV001078415
dbSNP Id: rs35165357

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226729dup , CM000673.2:g.5226729dup GRCh38
NC_000011.9:g.5247959dup , CM000673.1:g.5247959dup GRCh37
NC_000011.8:g.5204535dup NCBI36
NG_000007.3:g.70887dup
NG_059281.1:g.5343dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.163dup ENSP00000494175.1:p.Val55GlyfsTer6
ENST00000335295.4:c.163dup MANE Select ENSP00000333994.3:p.Val55GlyfsTer6
ENST00000380315.2:c.163dup ENSP00000369671.2:p.Val55GlyfsTer6
ENST00000475226.1:n.95dup
ENST00000485743.1:n.214dup
ENST00000633227.1:c.147dup ENSP00000488004.1:p.Leu50ValfsTer?
NM_000518.4:c.163dup NP_000509.1:p.Val55GlyfsTer6
NM_000518.5:c.163dup MANE Select NP_000509.1:p.Val55GlyfsTer6