Canonical Allele Identifier: CA2576666299

Gene: RNASEH1

Linked Data

• gnomAD v4: 2-3549134-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549134G>A , CM000664.2:g.3549134G>A	GRCh38
NC_000002.11:g.3596724G>A , CM000664.1:g.3596724G>A	GRCh37
NC_000002.10:g.3574599G>A	NCBI36
NG_051310.1:g.14238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.510-22C>T MANE Select	ENSP00000313350.3:n.510-22C>T
ENST00000654051.1:c.510-22C>T	ENSP00000499604.1:n.510-22C>T
ENST00000658393.1:c.510-22C>T	ENSP00000499330.1:n.510-22C>T
ENST00000315212.3:c.510-22C>T	ENSP00000313350.3:n.510-22C>T
ENST00000436842.5:c.*616-22C>T	ENSP00000404926.1:n.*616-22C>T
NM_001286834.1:c.432-22C>T	NP_001273763.1:n.432-22C>T
NM_001286837.1:c.159-22C>T	NP_001273766.1:n.159-22C>T
NM_002936.4:c.510-22C>T	NP_002927.2:n.510-22C>T
XR_244873.1:n.617-22C>T
XR_922665.1:n.617-22C>T
XR_922666.1:n.617-22C>T
XR_922667.1:n.617-22C>T
XR_922668.1:n.617-22C>T
XR_922669.1:n.617-22C>T
XR_922670.1:n.617-22C>T
XR_922671.1:n.617-22C>T
XR_922672.1:n.617-22C>T
XR_922673.1:n.617-22C>T
XR_922674.1:n.617-22C>T
NM_001286834.2:c.432-22C>T	NP_001273763.1:n.432-22C>T
NM_001286837.2:c.159-22C>T	NP_001273766.1:n.159-22C>T
NM_002936.5:c.510-22C>T	NP_002927.2:n.510-22C>T
NR_148532.1:n.621-22C>T
NR_148533.1:n.621-22C>T
NR_148534.1:n.621-22C>T
NM_001286837.3:c.159-22C>T	NP_001273766.1:n.159-22C>T
NR_148532.2:n.583-22C>T
NR_148533.2:n.583-22C>T
NR_148534.2:n.583-22C>T
NM_001286834.3:c.432-22C>T	NP_001273763.1:n.432-22C>T
NM_001378271.1:c.510-22C>T	NP_001365200.1:n.510-22C>T
NM_001378272.1:c.507-22C>T	NP_001365201.1:n.507-22C>T
NM_001378273.1:c.510-37C>T	NP_001365202.1:n.510-37C>T
NM_002936.6:c.510-22C>T MANE Select	NP_002927.2:n.510-22C>T
NR_165465.1:n.467-22C>T
NR_165466.1:n.583-53C>T
NR_165467.1:n.752-22C>T
NR_165468.1:n.555-22C>T