Canonical Allele Identifier: CA2838298644
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225503G>A , CM000673.2:g.5225503G>A GRCh38
NC_000011.9:g.5246733G>A , CM000673.1:g.5246733G>A GRCh37
NC_000011.8:g.5203309G>A NCBI36
NG_000007.3:g.72113C>T
NG_059281.1:g.6569C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.*95C>T ENSP00000494175.1:n.*95C>T
ENST00000335295.4:c.*95C>T MANE Select ENSP00000333994.3:n.*95C>T
ENST00000633227.1:c.*355C>T ENSP00000488004.1:n.*355C>T
NM_000518.4:c.*95C>T NP_000509.1:n.*95C>T
NM_000518.5:c.*95C>T MANE Select NP_000509.1:n.*95C>T