Canonical Allele Identifier: CA379273782
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226608T>G , CM000673.2:g.5226608T>G GRCh38
NC_000011.9:g.5247838T>G , CM000673.1:g.5247838T>G GRCh37
NC_000011.8:g.5204414T>G NCBI36
NG_000007.3:g.71008A>C
NG_059281.1:g.5464A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.284A>C ENSP00000494175.1:p.Asp95Ala
ENST00000335295.4:c.284A>C MANE Select ENSP00000333994.3:p.Asp95Ala
ENST00000475226.1:n.216A>C
ENST00000485743.1:n.335A>C
ENST00000633227.1:c.*100A>C ENSP00000488004.1:n.*100A>C
NM_000518.4:c.284A>C NP_000509.1:p.Asp95Ala
NM_000518.5:c.284A>C MANE Select NP_000509.1:p.Asp95Ala