Canonical Allele Identifier: CA1949565476
Gene: HBB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225750T= , CM000673.2:g.5225750T= GRCh38
NC_000011.9:g.5246980T= , CM000673.1:g.5246980T= GRCh37
NC_000011.8:g.5203556T= NCBI36
NG_000007.3:g.71866A=
NG_059281.1:g.6322A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.316-24A= ENSP00000494175.1:n.316-24A=
ENST00000335295.4:c.316-24A= MANE Select ENSP00000333994.3:n.316-24A=
ENST00000475226.1:n.248-24A=
ENST00000633227.1:c.*132-24A= ENSP00000488004.1:n.*132-24A=
NM_000518.4:c.316-24A= NP_000509.1:n.316-24A=
NM_000518.5:c.316-24A= MANE Select NP_000509.1:n.316-24A=
Search 100 bp 5'
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