Canonical Allele Identifier: CA217113388

Gene: HBB

Linked Data

• dbSNP Id: rs63750283
• MyVariant Identifiers: chr11:g.5247805A>T (hg19) ; chr11:g.5226575A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226575A>T , CM000673.2:g.5226575A>T	GRCh38
NC_000011.9:g.5247805A>T , CM000673.1:g.5247805A>T	GRCh37
NC_000011.8:g.5204381A>T	NCBI36
NG_000007.3:g.71041T>A
NG_059281.1:g.5497T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.315+2T>A	ENSP00000494175.1:n.315+2T>A
ENST00000335295.4:c.315+2T>A MANE Select	ENSP00000333994.3:n.315+2T>A
ENST00000475226.1:n.247+2T>A
ENST00000485743.1:n.368T>A
ENST00000633227.1:c.*131+2T>A	ENSP00000488004.1:n.*131+2T>A
NM_000518.4:c.315+2T>A	NP_000509.1:n.315+2T>A
NM_000518.5:c.315+2T>A MANE Select	NP_000509.1:n.315+2T>A