Canonical Allele Identifier: CA1949569542
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226782G= , CM000673.2:g.5226782G= GRCh38
NC_000011.9:g.5248012G= , CM000673.1:g.5248012G= GRCh37
NC_000011.8:g.5204588G= NCBI36
NG_000007.3:g.70834C=
NG_059281.1:g.5290C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.110C= ENSP00000494175.1:p.Pro37=
ENST00000335295.4:c.110C= MANE Select ENSP00000333994.3:p.Pro37=
ENST00000380315.2:c.110C= ENSP00000369671.2:p.Pro37=
ENST00000475226.1:n.42C=
ENST00000485743.1:n.161C=
ENST00000633227.1:c.94C= ENSP00000488004.1:p.Leu32=
NM_000518.4:c.110C= NP_000509.1:p.Pro37=
NM_000518.5:c.110C= MANE Select NP_000509.1:p.Pro37=