Canonical Allele Identifier: CA379273709

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5246906T>A (hg19) ; chr11:g.5225676T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225676T>A , CM000673.2:g.5225676T>A	GRCh38
NC_000011.9:g.5246906T>A , CM000673.1:g.5246906T>A	GRCh37
NC_000011.8:g.5203482T>A	NCBI36
NG_000007.3:g.71940A>T
NG_059281.1:g.6396A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.366A>T	ENSP00000494175.1:p.Glu122Asp
ENST00000335295.4:c.366A>T MANE Select	ENSP00000333994.3:p.Glu122Asp
ENST00000475226.1:n.298A>T
ENST00000633227.1:c.*182A>T	ENSP00000488004.1:n.*182A>T
NM_000518.4:c.366A>T	NP_000509.1:p.Glu122Asp
NM_000518.5:c.366A>T MANE Select	NP_000509.1:p.Glu122Asp