Canonical Allele Identifier: CA1949568813
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226719T= , CM000673.2:g.5226719T= GRCh38
NC_000011.9:g.5247949T= , CM000673.1:g.5247949T= GRCh37
NC_000011.8:g.5204525T= NCBI36
NG_000007.3:g.70897A=
NG_059281.1:g.5353A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.173A= ENSP00000494175.1:p.Asn58=
ENST00000335295.4:c.173A= MANE Select ENSP00000333994.3:p.Asn58=
ENST00000380315.2:c.173A= ENSP00000369671.2:p.Asn58=
ENST00000475226.1:n.105A=
ENST00000485743.1:n.224A=
ENST00000633227.1:c.157A= ENSP00000488004.1:p.Thr53=
NM_000518.4:c.173A= NP_000509.1:p.Asn58=
NM_000518.5:c.173A= MANE Select NP_000509.1:p.Asn58=