Canonical Allele Identifier: CA472638395

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5246891C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225661C>A , CM000673.2:g.5225661C>A	GRCh38
NC_000011.9:g.5246891C>A , CM000673.1:g.5246891C>A	GRCh37
NC_000011.8:g.5203467C>A	NCBI36
NG_000007.3:g.71955G>T
NG_059281.1:g.6411G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.381G>T	ENSP00000494175.1:p.Val127=
ENST00000335295.4:c.381G>T MANE Select	ENSP00000333994.3:p.Val127=
ENST00000475226.1:n.313G>T
ENST00000633227.1:c.*197G>T	ENSP00000488004.1:n.*197G>T
NM_000518.4:c.381G>T	NP_000509.1:p.Val127=
NM_000518.5:c.381G>T MANE Select	NP_000509.1:p.Val127=