Canonical Allele Identifier: CA379274509

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5247990C>G (hg19) ; chr11:g.5226760C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226760C>G , CM000673.2:g.5226760C>G	GRCh38
NC_000011.9:g.5247990C>G , CM000673.1:g.5247990C>G	GRCh37
NC_000011.8:g.5204566C>G	NCBI36
NG_000007.3:g.70856G>C
NG_059281.1:g.5312G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.132G>C	ENSP00000494175.1:p.Glu44Asp
ENST00000335295.4:c.132G>C MANE Select	ENSP00000333994.3:p.Glu44Asp
ENST00000380315.2:c.132G>C	ENSP00000369671.2:p.Glu44Asp
ENST00000475226.1:n.64G>C
ENST00000485743.1:n.183G>C
ENST00000633227.1:c.116G>C	ENSP00000488004.1:p.Ser39Thr
NM_000518.4:c.132G>C	NP_000509.1:p.Glu44Asp
NM_000518.5:c.132G>C MANE Select	NP_000509.1:p.Glu44Asp