Canonical Allele Identifier: CA379273640
Gene: HBB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225603G>T , CM000673.2:g.5225603G>T GRCh38
NC_000011.9:g.5246833G>T , CM000673.1:g.5246833G>T GRCh37
NC_000011.8:g.5203409G>T NCBI36
NG_000007.3:g.72013C>A
NG_059281.1:g.6469C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.439C>A ENSP00000494175.1:p.His147Asn
ENST00000335295.4:c.439C>A MANE Select ENSP00000333994.3:p.His147Asn
ENST00000633227.1:c.*255C>A ENSP00000488004.1:n.*255C>A
NM_000518.4:c.439C>A NP_000509.1:p.His147Asn
NM_000518.5:c.439C>A MANE Select NP_000509.1:p.His147Asn