Canonical Allele Identifier: CA345736963

Gene: RNASEH1

Linked Data

• MyVariant Identifiers: chr2:g.3596691A>T (hg19) ; chr2:g.3549101A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549101A>T , CM000664.2:g.3549101A>T	GRCh38
NC_000002.11:g.3596691A>T , CM000664.1:g.3596691A>T	GRCh37
NC_000002.10:g.3574566A>T	NCBI36
NG_051310.1:g.14271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.521T>A MANE Select	ENSP00000313350.3:p.Ile174Asn
ENST00000654051.1:c.521T>A	ENSP00000499604.1:p.Ile174Asn
ENST00000658393.1:c.521T>A	ENSP00000499330.1:p.Ile174Asn
ENST00000315212.3:c.521T>A	ENSP00000313350.3:p.Ile174Asn
ENST00000436842.5:c.*627T>A	ENSP00000404926.1:n.*627T>A
NM_001286834.1:c.443T>A	NP_001273763.1:p.Ile148Asn
NM_001286837.1:c.170T>A	NP_001273766.1:p.Ile57Asn
NM_002936.4:c.521T>A	NP_002927.2:p.Ile174Asn
XR_244873.1:n.628T>A
XR_922665.1:n.628T>A
XR_922666.1:n.628T>A
XR_922667.1:n.628T>A
XR_922668.1:n.628T>A
XR_922669.1:n.628T>A
XR_922670.1:n.628T>A
XR_922671.1:n.628T>A
XR_922672.1:n.628T>A
XR_922673.1:n.628T>A
XR_922674.1:n.628T>A
NM_001286834.2:c.443T>A	NP_001273763.1:p.Ile148Asn
NM_001286837.2:c.170T>A	NP_001273766.1:p.Ile57Asn
NM_002936.5:c.521T>A	NP_002927.2:p.Ile174Asn
NR_148532.1:n.632T>A
NR_148533.1:n.632T>A
NR_148534.1:n.632T>A
NM_001286837.3:c.170T>A	NP_001273766.1:p.Ile57Asn
NR_148532.2:n.594T>A
NR_148533.2:n.594T>A
NR_148534.2:n.594T>A
NM_001286834.3:c.443T>A	NP_001273763.1:p.Ile148Asn
NM_001378271.1:c.521T>A	NP_001365200.1:p.Ile174Asn
NM_001378272.1:c.518T>A	NP_001365201.1:p.Ile173Asn
NM_001378273.1:c.510-4T>A	NP_001365202.1:n.510-4T>A
NM_002936.6:c.521T>A MANE Select	NP_002927.2:p.Ile174Asn
NR_165465.1:n.478T>A
NR_165466.1:n.583-20T>A
NR_165467.1:n.763T>A
NR_165468.1:n.566T>A