Canonical Allele Identifier: CA1949568044
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226647A= , CM000673.2:g.5226647A= GRCh38
NC_000011.9:g.5247877A= , CM000673.1:g.5247877A= GRCh37
NC_000011.8:g.5204453A= NCBI36
NG_000007.3:g.70969T=
NG_059281.1:g.5425T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.245T= ENSP00000494175.1:p.Leu82=
ENST00000335295.4:c.245T= MANE Select ENSP00000333994.3:p.Leu82=
ENST00000380315.2:c.245T= ENSP00000369671.2:p.Leu82=
ENST00000475226.1:n.177T=
ENST00000485743.1:n.296T=
ENST00000633227.1:c.*61T= ENSP00000488004.1:n.*61T=
NM_000518.4:c.245T= NP_000509.1:p.Leu82=
NM_000518.5:c.245T= MANE Select NP_000509.1:p.Leu82=