Canonical Allele Identifier: CA2229026729

Gene: TERB1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66777305G= , CM000678.2:g.66777305G=	GRCh38
NC_000016.9:g.66811208G= , CM000678.1:g.66811208G=	GRCh37
NC_000016.8:g.65368709G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433154.6:c.883C= MANE Select	ENSP00000463762.1:p.His295=
ENST00000673664.1:c.850C=	ENSP00000500999.1:p.His284=
ENST00000313294.7:c.883C=	ENSP00000464579.1:p.His295=
ENST00000433154.5:c.883C=	ENSP00000463762.1:p.His295=
ENST00000558713.6:c.883C=	ENSP00000462883.1:p.His295=
ENST00000561333.1:n.1114C=
NM_001136505.1:c.883C=	NP_001129977.1:p.His295=
XM_011523004.1:c.883C=	XP_011521306.1:p.His295=
XM_011523005.1:c.883C=	XP_011521307.1:p.His295=
XM_011523006.1:c.883C=	XP_011521308.1:p.His295=
XM_011523007.1:c.883C=	XP_011521309.1:p.His295=
XM_011523008.1:c.883C=	XP_011521310.1:p.His295=
XM_011523009.1:c.883C=	XP_011521311.1:p.His295=
XM_011523010.1:c.850C=	XP_011521312.1:p.His284=
XM_011523011.1:c.850C=	XP_011521313.1:p.His284=
XM_011523012.1:c.850C=	XP_011521314.1:p.His284=
XM_011523013.1:c.754C=	XP_011521315.1:p.His252=
XM_011523014.1:c.883C=	XP_011521316.1:p.His295=
XM_011523015.1:c.883C=	XP_011521317.1:p.His295=
XM_011523016.1:c.883C=	XP_011521318.1:p.His295=
XM_011523017.1:c.883C=	XP_011521319.1:p.His295=
XM_011523018.1:c.883C=	XP_011521320.1:p.His295=
XM_011523019.1:c.883C=	XP_011521321.1:p.His295=
XM_011523020.1:c.883C=	XP_011521322.1:p.His295=
XR_933277.1:n.1145C=
XM_011523005.2:c.883C=	XP_011521307.1:p.His295=
XM_011523008.2:c.883C=	XP_011521310.1:p.His295=
XM_011523009.2:c.883C=	XP_011521311.1:p.His295=
XM_011523012.2:c.850C=	XP_011521314.1:p.His284=
NM_001136505.2:c.883C= MANE Select	NP_001129977.1:p.His295=