Canonical Allele Identifier: CA1949571394
Gene: HBB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227042A= , CM000673.2:g.5227042A= GRCh38
NC_000011.9:g.5248272A= , CM000673.1:g.5248272A= GRCh37
NC_000011.8:g.5204848A= NCBI36
NG_000007.3:g.70574T=
NG_059281.1:g.5030T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-21T= ENSP00000494175.1:n.-21T=
ENST00000335295.4:c.-21T= MANE Select ENSP00000333994.3:n.-21T=
ENST00000380315.2:c.-18-3T= ENSP00000369671.2:n.-18-3T=
ENST00000485743.1:n.31T=
ENST00000633227.1:c.-21T= ENSP00000488004.1:n.-21T=
NM_000518.4:c.-21T= NP_000509.1:n.-21T=
NM_000518.5:c.-21T= MANE Select NP_000509.1:n.-21T=
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