Canonical Allele Identifier: CA472885868

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5248213A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226983A>T , CM000673.2:g.5226983A>T	GRCh38
NC_000011.9:g.5248213A>T , CM000673.1:g.5248213A>T	GRCh37
NC_000011.8:g.5204789A>T	NCBI36
NG_000007.3:g.70633T>A
NG_059281.1:g.5089T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.39T>A	ENSP00000494175.1:p.Thr13=
ENST00000335295.4:c.39T>A MANE Select	ENSP00000333994.3:p.Thr13=
ENST00000380315.2:c.39T>A	ENSP00000369671.2:p.Thr13=
ENST00000485743.1:n.90T>A
ENST00000633227.1:c.39T>A	ENSP00000488004.1:p.Thr13=
NM_000518.4:c.39T>A	NP_000509.1:p.Thr13=
NM_000518.5:c.39T>A MANE Select	NP_000509.1:p.Thr13=