Canonical Allele Identifier: CA217114368

Gene: HBB

Linked Data

• dbSNP Id: rs33980484
• MyVariant Identifiers: chr11:g.5247979T>A (hg19) ; chr11:g.5226749T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226749T>A , CM000673.2:g.5226749T>A	GRCh38
NC_000011.9:g.5247979T>A , CM000673.1:g.5247979T>A	GRCh37
NC_000011.8:g.5204555T>A	NCBI36
NG_000007.3:g.70867A>T
NG_059281.1:g.5323A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.143A>T	ENSP00000494175.1:p.Asp48Val
ENST00000335295.4:c.143A>T MANE Select	ENSP00000333994.3:p.Asp48Val
ENST00000380315.2:c.143A>T	ENSP00000369671.2:p.Asp48Val
ENST00000475226.1:n.75A>T
ENST00000485743.1:n.194A>T
ENST00000633227.1:c.127A>T	ENSP00000488004.1:p.Ile43Phe
NM_000518.4:c.143A>T	NP_000509.1:p.Asp48Val
NM_000518.5:c.143A>T MANE Select	NP_000509.1:p.Asp48Val