Canonical Allele Identifier: CA420192531

Gene: WARS2

Linked Data

• dbSNP Id: rs1369223570
• gnomAD v2: 1-119575777-G-C
• gnomAD v4: 1-119033154-G-C
• MyVariant Identifiers: chr1:g.119575777G>C (hg19) ; chr1:g.119033154G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033154G>C , CM000663.2:g.119033154G>C	GRCh38
NC_000001.10:g.119575777G>C , CM000663.1:g.119575777G>C	GRCh37
NC_000001.9:g.119377300G>C	NCBI36
NG_050658.1:g.112635C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.840C>G MANE Select	ENSP00000235521.4:p.Ala280=
ENST00000235521.4:c.840C>G	ENSP00000235521.4:p.Ala280=
ENST00000369426.9:c.*206C>G	ENSP00000358434.5:n.*206C>G
NM_015836.3:c.840C>G	NP_056651.1:p.Ala280=
NM_201263.2:c.*206C>G	NP_957715.1:n.*206C>G
XM_005270350.2:c.786C>G	XP_005270407.1:p.Ala262=
XM_006710283.1:c.558C>G	XP_006710346.1:p.Ala186=
XM_011540493.1:c.771C>G	XP_011538795.1:p.Ala257=
XM_011540494.1:c.771C>G	XP_011538796.1:p.Ala257=
XM_011540495.1:c.582C>G	XP_011538797.1:p.Ala194=
XM_005270350.3:c.786C>G	XP_005270407.1:p.Ala262=
XM_011540494.2:c.771C>G	XP_011538796.1:p.Ala257=
XM_011540495.2:c.582C>G	XP_011538797.1:p.Ala194=
XM_017000038.1:c.783C>G	XP_016855527.1:p.Ala261=
XM_017000039.1:c.771C>G	XP_016855528.1:p.Ala257=
XM_017000040.1:c.669C>G	XP_016855529.1:p.Ala223=
XM_017000041.2:c.501C>G	XP_016855530.1:p.Ala167=
XM_017000042.1:c.*175C>G	XP_016855531.1:n.*175C>G
XM_024449826.1:c.771C>G	XP_024305594.1:p.Ala257=
XM_024449860.1:c.558C>G	XP_024305628.1:p.Ala186=
XM_024449871.1:c.558C>G	XP_024305639.1:p.Ala186=
NM_001378226.1:c.771C>G	NP_001365155.1:p.Ala257=
NM_001378227.1:c.771C>G	NP_001365156.1:p.Ala257=
NM_001378228.1:c.669C>G	NP_001365157.1:p.Ala223=
NM_001378229.1:c.582C>G	NP_001365158.1:p.Ala194=
NM_001378230.1:c.558C>G	NP_001365159.1:p.Ala186=
NM_001378231.1:c.*175C>G	NP_001365160.1:n.*175C>G
NM_015836.4:c.840C>G MANE Select	NP_056651.1:p.Ala280=