Canonical Allele Identifier: CA2580084017
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 2030369
ClinVar RCV Id: RCV002871743

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226830A>C , CM000673.2:g.5226830A>C GRCh38
NC_000011.9:g.5248060A>C , CM000673.1:g.5248060A>C GRCh37
NC_000011.8:g.5204636A>C NCBI36
NG_000007.3:g.70786T>G
NG_059281.1:g.5242T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.93-31T>G ENSP00000494175.1:n.93-31T>G
ENST00000335295.4:c.93-31T>G MANE Select ENSP00000333994.3:n.93-31T>G
ENST00000380315.2:c.93-31T>G ENSP00000369671.2:n.93-31T>G
ENST00000485743.1:n.144-31T>G
ENST00000633227.1:c.77-31T>G ENSP00000488004.1:n.77-31T>G
NM_000518.4:c.93-31T>G NP_000509.1:n.93-31T>G
NM_000518.5:c.93-31T>G MANE Select NP_000509.1:n.93-31T>G