Canonical Allele Identifier: CA345736895

Gene: RNASEH1

Linked Data

• gnomAD v4: 2-3549069-C-T
• MyVariant Identifiers: chr2:g.3596659C>T (hg19) ; chr2:g.3549069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549069C>T , CM000664.2:g.3549069C>T	GRCh38
NC_000002.11:g.3596659C>T , CM000664.1:g.3596659C>T	GRCh37
NC_000002.10:g.3574534C>T	NCBI36
NG_051310.1:g.14303G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000315212.4:c.553G>A MANE Select	ENSP00000313350.3:p.Ala185Thr
ENST00000654051.1:c.553G>A	ENSP00000499604.1:p.Ala185Thr
ENST00000658393.1:c.553G>A	ENSP00000499330.1:p.Ala185Thr
ENST00000315212.3:c.553G>A	ENSP00000313350.3:p.Ala185Thr
ENST00000436842.5:c.*659G>A	ENSP00000404926.1:n.*659G>A
NM_001286834.1:c.475G>A	NP_001273763.1:p.Ala159Thr
NM_001286837.1:c.202G>A	NP_001273766.1:p.Ala68Thr
NM_002936.4:c.553G>A	NP_002927.2:p.Ala185Thr
XR_244873.1:n.660G>A
XR_922665.1:n.660G>A
XR_922666.1:n.660G>A
XR_922667.1:n.660G>A
XR_922668.1:n.660G>A
XR_922669.1:n.660G>A
XR_922670.1:n.660G>A
XR_922671.1:n.660G>A
XR_922672.1:n.660G>A
XR_922673.1:n.660G>A
XR_922674.1:n.660G>A
NM_001286834.2:c.475G>A	NP_001273763.1:p.Ala159Thr
NM_001286837.2:c.202G>A	NP_001273766.1:p.Ala68Thr
NM_002936.5:c.553G>A	NP_002927.2:p.Ala185Thr
NR_148532.1:n.664G>A
NR_148533.1:n.664G>A
NR_148534.1:n.664G>A
NM_001286837.3:c.202G>A	NP_001273766.1:p.Ala68Thr
NR_148532.2:n.626G>A
NR_148533.2:n.626G>A
NR_148534.2:n.626G>A
NM_001286834.3:c.475G>A	NP_001273763.1:p.Ala159Thr
NM_001378271.1:c.553G>A	NP_001365200.1:p.Ala185Thr
NM_001378272.1:c.550G>A	NP_001365201.1:p.Ala184Thr
NM_001378273.1:c.538G>A	NP_001365202.1:p.Ala180Thr
NM_002936.6:c.553G>A MANE Select	NP_002927.2:p.Ala185Thr
NR_165465.1:n.510G>A
NR_165466.1:n.595G>A
NR_165467.1:n.795G>A
NR_165468.1:n.598G>A