Canonical Allele Identifier: CA379273774

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5247833G>T (hg19) ; chr11:g.5226603G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226603G>T , CM000673.2:g.5226603G>T	GRCh38
NC_000011.9:g.5247833G>T , CM000673.1:g.5247833G>T	GRCh37
NC_000011.8:g.5204409G>T	NCBI36
NG_000007.3:g.71013C>A
NG_059281.1:g.5469C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.289C>A	ENSP00000494175.1:p.Leu97Met
ENST00000335295.4:c.289C>A MANE Select	ENSP00000333994.3:p.Leu97Met
ENST00000475226.1:n.221C>A
ENST00000485743.1:n.340C>A
ENST00000633227.1:c.*105C>A	ENSP00000488004.1:n.*105C>A
NM_000518.4:c.289C>A	NP_000509.1:p.Leu97Met
NM_000518.5:c.289C>A MANE Select	NP_000509.1:p.Leu97Met