Canonical Allele Identifier: CA934687479
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226367_5226372dup , CM000673.2:g.5226367_5226372dup GRCh38
NC_000011.9:g.5247597_5247602dup , CM000673.1:g.5247597_5247602dup GRCh37
NC_000011.8:g.5204173_5204178dup NCBI36
NG_000007.3:g.71247_71252dup
NG_059281.1:g.5703_5708dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.315+208_315+213dup ENSP00000494175.1:n.315+208_315+213dup
ENST00000335295.4:c.315+208_315+213dup MANE Select ENSP00000333994.3:n.315+208_315+213dup
ENST00000475226.1:n.247+208_247+213dup
ENST00000485743.1:n.574_579dup
ENST00000633227.1:c.*131+208_*131+213dup ENSP00000488004.1:n.*131+208_*131+213dup
NM_000518.4:c.315+208_315+213dup NP_000509.1:n.315+208_315+213dup
NM_000518.5:c.315+208_315+213dup MANE Select NP_000509.1:n.315+208_315+213dup