Canonical Allele Identifier: CA472885863

Gene: HBB

Linked Data

• MyVariant Identifiers: chr11:g.5248210G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226980G>A , CM000673.2:g.5226980G>A	GRCh38
NC_000011.9:g.5248210G>A , CM000673.1:g.5248210G>A	GRCh37
NC_000011.8:g.5204786G>A	NCBI36
NG_000007.3:g.70636C>T
NG_059281.1:g.5092C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.42C>T	ENSP00000494175.1:p.Ala14=
ENST00000335295.4:c.42C>T MANE Select	ENSP00000333994.3:p.Ala14=
ENST00000380315.2:c.42C>T	ENSP00000369671.2:p.Ala14=
ENST00000485743.1:n.93C>T
ENST00000633227.1:c.42C>T	ENSP00000488004.1:p.Ala14=
NM_000518.4:c.42C>T	NP_000509.1:p.Ala14=
NM_000518.5:c.42C>T MANE Select	NP_000509.1:p.Ala14=