Canonical Allele Identifier: CA345736874

Gene: RNASEH1

Linked Data

• MyVariant Identifiers: chr2:g.3596650G>C (hg19) ; chr2:g.3549060G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549060G>C , CM000664.2:g.3549060G>C	GRCh38
NC_000002.11:g.3596650G>C , CM000664.1:g.3596650G>C	GRCh37
NC_000002.10:g.3574525G>C	NCBI36
NG_051310.1:g.14312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.562C>G MANE Select	ENSP00000313350.3:p.His188Asp
ENST00000654051.1:c.562C>G	ENSP00000499604.1:p.His188Asp
ENST00000658393.1:c.562C>G	ENSP00000499330.1:p.His188Asp
ENST00000315212.3:c.562C>G	ENSP00000313350.3:p.His188Asp
ENST00000436842.5:c.*668C>G	ENSP00000404926.1:n.*668C>G
NM_001286834.1:c.484C>G	NP_001273763.1:p.His162Asp
NM_001286837.1:c.211C>G	NP_001273766.1:p.His71Asp
NM_002936.4:c.562C>G	NP_002927.2:p.His188Asp
XR_244873.1:n.669C>G
XR_922665.1:n.669C>G
XR_922666.1:n.669C>G
XR_922667.1:n.669C>G
XR_922668.1:n.669C>G
XR_922669.1:n.669C>G
XR_922670.1:n.669C>G
XR_922671.1:n.669C>G
XR_922672.1:n.669C>G
XR_922673.1:n.669C>G
XR_922674.1:n.669C>G
NM_001286834.2:c.484C>G	NP_001273763.1:p.His162Asp
NM_001286837.2:c.211C>G	NP_001273766.1:p.His71Asp
NM_002936.5:c.562C>G	NP_002927.2:p.His188Asp
NR_148532.1:n.673C>G
NR_148533.1:n.673C>G
NR_148534.1:n.673C>G
NM_001286837.3:c.211C>G	NP_001273766.1:p.His71Asp
NR_148532.2:n.635C>G
NR_148533.2:n.635C>G
NR_148534.2:n.635C>G
NM_001286834.3:c.484C>G	NP_001273763.1:p.His162Asp
NM_001378271.1:c.562C>G	NP_001365200.1:p.His188Asp
NM_001378272.1:c.559C>G	NP_001365201.1:p.His187Asp
NM_001378273.1:c.547C>G	NP_001365202.1:p.His183Asp
NM_002936.6:c.562C>G MANE Select	NP_002927.2:p.His188Asp
NR_165465.1:n.519C>G
NR_165466.1:n.604C>G
NR_165467.1:n.804C>G
NR_165468.1:n.607C>G