Canonical Allele Identifier: CA223999428
Gene: RNASEH2C HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65720176G>T , CM000673.2:g.65720176G>T GRCh38
NC_000011.9:g.65487647G>T , CM000673.1:g.65487647G>T GRCh37
NC_000011.8:g.65244223G>T NCBI36
NG_008976.2:g.5763C>A , LRG_280:g.5763C>A
NG_033057.1:g.13175G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308418.10:c.349-12C>A MANE Select ENSP00000308193.5:n.349-12C>A
ENST00000528220.2:n.578-12C>A
ENST00000531596.6:c.349-12C>A ENSP00000435717.2:n.349-12C>A
ENST00000534482.6:c.349-12C>A ENSP00000432081.2:n.349-12C>A
ENST00000642430.1:n.242-12C>A
ENST00000643214.1:n.411C>A
ENST00000644142.1:c.349-12C>A ENSP00000493695.1:n.349-12C>A
ENST00000644198.1:n.246-12C>A
ENST00000646597.1:n.286-12C>A
ENST00000308418.8:c.349-12C>A ENSP00000308193.4:n.349-12C>A
ENST00000527610.1:c.349-12C>A ENSP00000432897.1:n.349-12C>A
ENST00000528220.1:c.100-12C>A ENSP00000431555.1:n.100-12C>A
ENST00000530192.1:n.454C>A
ENST00000531596.5:c.330-12C>A
ENST00000533698.5:c.228-12C>A
ENST00000534482.5:c.243-12C>A
NM_032193.3:c.349-12C>A , LRG_280t1:c.349-12C>A NP_115569.2:n.349-12C>A
NM_032193.4:c.349-12C>A MANE Select NP_115569.2:n.349-12C>A