Canonical Allele Identifier: CA224000270
Gene: RNASEH2C HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000308418.10:c.38G>A MANE Select ENSP00000308193.5:p.Arg13His
ENST00000528220.2:n.98G>A
ENST00000531596.6:c.38G>A ENSP00000435717.2:p.Arg13His
ENST00000534482.6:c.38G>A ENSP00000432081.2:p.Arg13His
ENST00000644142.1:c.38G>A ENSP00000493695.1:p.Arg13His
ENST00000308418.8:c.38G>A ENSP00000308193.4:p.Arg13His
ENST00000527610.1:c.38G>A ENSP00000432897.1:p.Arg13His
ENST00000528220.1:c.-381G>A ENSP00000431555.1:n.-381G>A
ENST00000530192.1:n.78G>A
ENST00000531596.5:c.19G>A
NM_032193.3:c.38G>A , LRG_280t1:c.38G>A NP_115569.2:p.Arg13His
NM_032193.4:c.38G>A MANE Select NP_115569.2:p.Arg13His
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Search 100 bp 3'