Canonical Allele Identifier: CA381299010

Gene: RNASEH2C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65720385G>C , CM000673.2:g.65720385G>C	GRCh38
NC_000011.9:g.65487856G>C , CM000673.1:g.65487856G>C	GRCh37
NC_000011.8:g.65244432G>C	NCBI36
NG_008976.2:g.5554C>G , LRG_280:g.5554C>G
NG_033057.1:g.13384G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032193.4:c.205C>G MANE Select	NP_115569.2:p.Arg69Gly
ENST00000308418.10:c.205C>G MANE Select	ENSP00000308193.5:p.Arg69Gly
NM_032193.3:c.205C>G , LRG_280t1:c.205C>G	NP_115569.2:p.Arg69Gly
ENST00000308418.8:c.205C>G	ENSP00000308193.4:p.Arg69Gly
ENST00000527610.1:c.205C>G	ENSP00000432897.1:p.Arg69Gly
ENST00000528220.1:c.-45C>G	ENSP00000431555.1:n.-45C>G
ENST00000528220.2:n.434C>G
ENST00000530192.1:n.245C>G
ENST00000531596.5:c.186C>G
ENST00000531596.6:c.205C>G	ENSP00000435717.2:p.Arg69Gly
ENST00000533698.5:c.84C>G
ENST00000534482.5:c.99C>G
ENST00000534482.6:c.205C>G	ENSP00000432081.2:p.Arg69Gly
ENST00000642430.1:n.98C>G
ENST00000643214.1:n.202C>G
ENST00000644142.1:c.205C>G	ENSP00000493695.1:p.Arg69Gly
ENST00000644198.1:n.102C>G
ENST00000646597.1:n.142C>G