Canonical Allele Identifier: CA379273845

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5247900A>T (hg19) ; chr11:g.5226670A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226670A>T , CM000673.2:g.5226670A>T	GRCh38
NC_000011.9:g.5247900A>T , CM000673.1:g.5247900A>T	GRCh37
NC_000011.8:g.5204476A>T	NCBI36
NG_000007.3:g.70946T>A
NG_059281.1:g.5402T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.222T>A	ENSP00000494175.1:p.Asp74Glu
ENST00000335295.4:c.222T>A MANE Select	ENSP00000333994.3:p.Asp74Glu
ENST00000380315.2:c.222T>A	ENSP00000369671.2:p.Asp74Glu
ENST00000475226.1:n.154T>A
ENST00000485743.1:n.273T>A
ENST00000633227.1:c.*38T>A	ENSP00000488004.1:n.*38T>A
NM_000518.4:c.222T>A	NP_000509.1:p.Asp74Glu
NM_000518.5:c.222T>A MANE Select	NP_000509.1:p.Asp74Glu