Canonical Allele Identifier: CA2507821955

Gene: RNASEH1

Linked Data

• gnomAD v4: 2-3548967-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3548967T>C , CM000664.2:g.3548967T>C	GRCh38
NC_000002.11:g.3596557T>C , CM000664.1:g.3596557T>C	GRCh37
NC_000002.10:g.3574432T>C	NCBI36
NG_051310.1:g.14405A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.564+91A>G MANE Select	ENSP00000313350.3:n.564+91A>G
ENST00000654051.1:c.564+91A>G	ENSP00000499604.1:n.564+91A>G
ENST00000658393.1:c.564+91A>G	ENSP00000499330.1:n.564+91A>G
ENST00000315212.3:c.564+91A>G	ENSP00000313350.3:n.564+91A>G
ENST00000436842.5:c.*670+91A>G	ENSP00000404926.1:n.*670+91A>G
NM_001286834.1:c.486+91A>G	NP_001273763.1:n.486+91A>G
NM_001286837.1:c.213+91A>G	NP_001273766.1:n.213+91A>G
NM_002936.4:c.564+91A>G	NP_002927.2:n.564+91A>G
XR_244873.1:n.671+91A>G
XR_922665.1:n.671+91A>G
XR_922666.1:n.671+91A>G
XR_922667.1:n.671+91A>G
XR_922668.1:n.671+91A>G
XR_922669.1:n.671+91A>G
XR_922670.1:n.671+91A>G
XR_922671.1:n.671+91A>G
XR_922672.1:n.671+91A>G
XR_922673.1:n.671+91A>G
XR_922674.1:n.671+91A>G
NM_001286834.2:c.486+91A>G	NP_001273763.1:n.486+91A>G
NM_001286837.2:c.213+91A>G	NP_001273766.1:n.213+91A>G
NM_002936.5:c.564+91A>G	NP_002927.2:n.564+91A>G
NR_148532.1:n.675+91A>G
NR_148533.1:n.675+91A>G
NR_148534.1:n.675+91A>G
NM_001286837.3:c.213+91A>G	NP_001273766.1:n.213+91A>G
NR_148532.2:n.637+91A>G
NR_148533.2:n.637+91A>G
NR_148534.2:n.637+91A>G
NM_001286834.3:c.486+91A>G	NP_001273763.1:n.486+91A>G
NM_001378271.1:c.564+91A>G	NP_001365200.1:n.564+91A>G
NM_001378272.1:c.561+91A>G	NP_001365201.1:n.561+91A>G
NM_001378273.1:c.549+91A>G	NP_001365202.1:n.549+91A>G
NM_002936.6:c.564+91A>G MANE Select	NP_002927.2:n.564+91A>G
NR_165465.1:n.521+91A>G
NR_165466.1:n.606+91A>G
NR_165467.1:n.806+91A>G
NR_165468.1:n.609+91A>G