Canonical Allele Identifier: CA1035207

Gene: WARS2

Linked Data

• dbSNP Id: rs755664136
• ExAC: 1:119575780 A / G
• gnomAD v2: 1-119575780-A-G
• gnomAD v3: 1-119033157-A-G
• gnomAD v4: 1-119033157-A-G
• MyVariant Identifiers: chr1:g.119575780A>G (hg19) ; chr1:g.119033157A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033157A>G , CM000663.2:g.119033157A>G	GRCh38
NC_000001.10:g.119575780A>G , CM000663.1:g.119575780A>G	GRCh37
NC_000001.9:g.119377303A>G	NCBI36
NG_050658.1:g.112632T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.837T>C MANE Select	ENSP00000235521.4:p.His279=
ENST00000235521.4:c.837T>C	ENSP00000235521.4:p.His279=
ENST00000369426.9:c.*203T>C	ENSP00000358434.5:n.*203T>C
NM_015836.3:c.837T>C	NP_056651.1:p.His279=
NM_201263.2:c.*203T>C	NP_957715.1:n.*203T>C
XM_005270350.2:c.783T>C	XP_005270407.1:p.His261=
XM_006710283.1:c.555T>C	XP_006710346.1:p.His185=
XM_011540493.1:c.768T>C	XP_011538795.1:p.His256=
XM_011540494.1:c.768T>C	XP_011538796.1:p.His256=
XM_011540495.1:c.579T>C	XP_011538797.1:p.His193=
XM_005270350.3:c.783T>C	XP_005270407.1:p.His261=
XM_011540494.2:c.768T>C	XP_011538796.1:p.His256=
XM_011540495.2:c.579T>C	XP_011538797.1:p.His193=
XM_017000038.1:c.780T>C	XP_016855527.1:p.His260=
XM_017000039.1:c.768T>C	XP_016855528.1:p.His256=
XM_017000040.1:c.666T>C	XP_016855529.1:p.His222=
XM_017000041.2:c.498T>C	XP_016855530.1:p.His166=
XM_017000042.1:c.*172T>C	XP_016855531.1:n.*172T>C
XM_024449826.1:c.768T>C	XP_024305594.1:p.His256=
XM_024449860.1:c.555T>C	XP_024305628.1:p.His185=
XM_024449871.1:c.555T>C	XP_024305639.1:p.His185=
NM_001378226.1:c.768T>C	NP_001365155.1:p.His256=
NM_001378227.1:c.768T>C	NP_001365156.1:p.His256=
NM_001378228.1:c.666T>C	NP_001365157.1:p.His222=
NM_001378229.1:c.579T>C	NP_001365158.1:p.His193=
NM_001378230.1:c.555T>C	NP_001365159.1:p.His185=
NM_001378231.1:c.*172T>C	NP_001365160.1:n.*172T>C
NM_015836.4:c.837T>C MANE Select	NP_056651.1:p.His279=