Canonical Allele Identifier: CA1949567451
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226590G= , CM000673.2:g.5226590G= GRCh38
NC_000011.9:g.5247820G= , CM000673.1:g.5247820G= GRCh37
NC_000011.8:g.5204396G= NCBI36
NG_000007.3:g.71026C=
NG_059281.1:g.5482C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.302C= ENSP00000494175.1:p.Pro101=
ENST00000335295.4:c.302C= MANE Select ENSP00000333994.3:p.Pro101=
ENST00000475226.1:n.234C=
ENST00000485743.1:n.353C=
ENST00000633227.1:c.*118C= ENSP00000488004.1:n.*118C=
NM_000518.4:c.302C= NP_000509.1:p.Pro101=
NM_000518.5:c.302C= MANE Select NP_000509.1:p.Pro101=