Canonical Allele Identifier: CA472638516
Gene: HBB HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.5246929G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225699G>A , CM000673.2:g.5225699G>A GRCh38
NC_000011.9:g.5246929G>A , CM000673.1:g.5246929G>A GRCh37
NC_000011.8:g.5203505G>A NCBI36
NG_000007.3:g.71917C>T
NG_059281.1:g.6373C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.343C>T ENSP00000494175.1:p.Leu115=
ENST00000335295.4:c.343C>T MANE Select ENSP00000333994.3:p.Leu115=
ENST00000475226.1:n.275C>T
ENST00000633227.1:c.*159C>T ENSP00000488004.1:n.*159C>T
NM_000518.4:c.343C>T NP_000509.1:p.Leu115=
NM_000518.5:c.343C>T MANE Select NP_000509.1:p.Leu115=