Canonical Allele Identifier: CA1949571448
Gene: HBB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5227052G= , CM000673.2:g.5227052G= GRCh38
NC_000011.9:g.5248282G= , CM000673.1:g.5248282G= GRCh37
NC_000011.8:g.5204858G= NCBI36
NG_000007.3:g.70564C=
NG_059281.1:g.5020C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.-31C= ENSP00000494175.1:n.-31C=
ENST00000335295.4:c.-31C= MANE Select ENSP00000333994.3:n.-31C=
ENST00000380315.2:c.-18-13C= ENSP00000369671.2:n.-18-13C=
ENST00000485743.1:n.21C=
ENST00000633227.1:c.-31C= ENSP00000488004.1:n.-31C=
NM_000518.4:c.-31C= NP_000509.1:n.-31C=
NM_000518.5:c.-31C= MANE Select NP_000509.1:n.-31C=
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