Canonical Allele Identifier: CA1949568029
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226646G= , CM000673.2:g.5226646G= GRCh38
NC_000011.9:g.5247876G= , CM000673.1:g.5247876G= GRCh37
NC_000011.8:g.5204452G= NCBI36
NG_000007.3:g.70970C=
NG_059281.1:g.5426C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.246C= ENSP00000494175.1:p.Leu82=
ENST00000335295.4:c.246C= MANE Select ENSP00000333994.3:p.Leu82=
ENST00000380315.2:c.246C= ENSP00000369671.2:p.Leu82=
ENST00000475226.1:n.178C=
ENST00000485743.1:n.297C=
ENST00000633227.1:c.*62C= ENSP00000488004.1:n.*62C=
NM_000518.4:c.246C= NP_000509.1:p.Leu82=
NM_000518.5:c.246C= MANE Select NP_000509.1:p.Leu82=