Canonical Allele Identifier: CA6107740

Gene: RNASEH2C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65720281C>G , CM000673.2:g.65720281C>G	GRCh38
NC_000011.9:g.65487752C>G , CM000673.1:g.65487752C>G	GRCh37
NC_000011.8:g.65244328C>G	NCBI36
NG_008976.2:g.5658G>C , LRG_280:g.5658G>C
NG_033057.1:g.13280C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032193.4:c.309G>C MANE Select	NP_115569.2:p.Gly103=
ENST00000308418.10:c.309G>C MANE Select	ENSP00000308193.5:p.Gly103=
NM_032193.3:c.309G>C , LRG_280t1:c.309G>C	NP_115569.2:p.Gly103=
ENST00000308418.8:c.309G>C	ENSP00000308193.4:p.Gly103=
ENST00000527610.1:c.309G>C	ENSP00000432897.1:p.Gly103=
ENST00000528220.1:c.60G>C	ENSP00000431555.1:p.Gly20=
ENST00000528220.2:n.538G>C
ENST00000530192.1:n.349G>C
ENST00000531596.5:c.290G>C
ENST00000531596.6:c.309G>C	ENSP00000435717.2:p.Gly103=
ENST00000533698.5:c.188G>C
ENST00000534482.5:c.203G>C
ENST00000534482.6:c.309G>C	ENSP00000432081.2:p.Gly103=
ENST00000642430.1:n.202G>C
ENST00000643214.1:n.306G>C
ENST00000644142.1:c.309G>C	ENSP00000493695.1:p.Gly103=
ENST00000644198.1:n.206G>C
ENST00000646597.1:n.246G>C