Canonical Allele Identifier: CA379274640
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226797A>T , CM000673.2:g.5226797A>T GRCh38
NC_000011.9:g.5248027A>T , CM000673.1:g.5248027A>T GRCh37
NC_000011.8:g.5204603A>T NCBI36
NG_000007.3:g.70819T>A
NG_059281.1:g.5275T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.95T>A ENSP00000494175.1:p.Leu32Gln
ENST00000335295.4:c.95T>A MANE Select ENSP00000333994.3:p.Leu32Gln
ENST00000380315.2:c.95T>A ENSP00000369671.2:p.Leu32Gln
ENST00000475226.1:n.27T>A
ENST00000485743.1:n.146T>A
ENST00000633227.1:c.79T>A ENSP00000488004.1:p.Cys27Ser
NM_000518.4:c.95T>A NP_000509.1:p.Leu32Gln
NM_000518.5:c.95T>A MANE Select NP_000509.1:p.Leu32Gln