Canonical Allele Identifier: CA1949563809
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225517T= , CM000673.2:g.5225517T= GRCh38
NC_000011.9:g.5246747T= , CM000673.1:g.5246747T= GRCh37
NC_000011.8:g.5203323T= NCBI36
NG_000007.3:g.72099A=
NG_059281.1:g.6555A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.*81A= ENSP00000494175.1:n.*81A=
ENST00000335295.4:c.*81A= MANE Select ENSP00000333994.3:n.*81A=
ENST00000633227.1:c.*341A= ENSP00000488004.1:n.*341A=
NM_000518.4:c.*81A= NP_000509.1:n.*81A=
NM_000518.5:c.*81A= MANE Select NP_000509.1:n.*81A=