Canonical Allele Identifier: CA424594395

Gene: RNASEH1

Linked Data

• gnomAD v4: 2-3549091-A-T
• MyVariant Identifiers: chr2:g.3596681A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.3549091A>T , CM000664.2:g.3549091A>T	GRCh38
NC_000002.11:g.3596681A>T , CM000664.1:g.3596681A>T	GRCh37
NC_000002.10:g.3574556A>T	NCBI36
NG_051310.1:g.14281T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315212.4:c.531T>A MANE Select	ENSP00000313350.3:p.Pro177=
ENST00000654051.1:c.531T>A	ENSP00000499604.1:p.Pro177=
ENST00000658393.1:c.531T>A	ENSP00000499330.1:p.Pro177=
ENST00000315212.3:c.531T>A	ENSP00000313350.3:p.Pro177=
ENST00000436842.5:c.*637T>A	ENSP00000404926.1:n.*637T>A
NM_001286834.1:c.453T>A	NP_001273763.1:p.Pro151=
NM_001286837.1:c.180T>A	NP_001273766.1:p.Pro60=
NM_002936.4:c.531T>A	NP_002927.2:p.Pro177=
XR_244873.1:n.638T>A
XR_922665.1:n.638T>A
XR_922666.1:n.638T>A
XR_922667.1:n.638T>A
XR_922668.1:n.638T>A
XR_922669.1:n.638T>A
XR_922670.1:n.638T>A
XR_922671.1:n.638T>A
XR_922672.1:n.638T>A
XR_922673.1:n.638T>A
XR_922674.1:n.638T>A
NM_001286834.2:c.453T>A	NP_001273763.1:p.Pro151=
NM_001286837.2:c.180T>A	NP_001273766.1:p.Pro60=
NM_002936.5:c.531T>A	NP_002927.2:p.Pro177=
NR_148532.1:n.642T>A
NR_148533.1:n.642T>A
NR_148534.1:n.642T>A
NM_001286837.3:c.180T>A	NP_001273766.1:p.Pro60=
NR_148532.2:n.604T>A
NR_148533.2:n.604T>A
NR_148534.2:n.604T>A
NM_001286834.3:c.453T>A	NP_001273763.1:p.Pro151=
NM_001378271.1:c.531T>A	NP_001365200.1:p.Pro177=
NM_001378272.1:c.528T>A	NP_001365201.1:p.Pro176=
NM_001378273.1:c.516T>A	NP_001365202.1:p.Pro172=
NM_002936.6:c.531T>A MANE Select	NP_002927.2:p.Pro177=
NR_165465.1:n.488T>A
NR_165466.1:n.583-10T>A
NR_165467.1:n.773T>A
NR_165468.1:n.576T>A