Canonical Allele Identifier: CA1979336967

Gene: RNASEH2C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65720721C= , CM000673.2:g.65720721C=	GRCh38
NC_000011.9:g.65488192C= , CM000673.1:g.65488192C=	GRCh37
NC_000011.8:g.65244768C=	NCBI36
NG_008976.2:g.5218G= , LRG_280:g.5218G=
NG_033057.1:g.13720C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032193.4:c.38G= MANE Select	NP_115569.2:p.Arg13=
ENST00000308418.10:c.38G= MANE Select	ENSP00000308193.5:p.Arg13=
NM_032193.3:c.38G= , LRG_280t1:c.38G=	NP_115569.2:p.Arg13=
ENST00000308418.8:c.38G=	ENSP00000308193.4:p.Arg13=
ENST00000527610.1:c.38G=	ENSP00000432897.1:p.Arg13=
ENST00000528220.1:c.-381G=	ENSP00000431555.1:n.-381G=
ENST00000528220.2:n.98G=
ENST00000530192.1:n.78G=
ENST00000531596.5:c.19G=
ENST00000531596.6:c.38G=	ENSP00000435717.2:p.Arg13=
ENST00000534482.6:c.38G=	ENSP00000432081.2:p.Arg13=
ENST00000644142.1:c.38G=	ENSP00000493695.1:p.Arg13=