Canonical Allele Identifier: CA1192170756

Gene: WARS2

Linked Data

• dbSNP Id: rs1656864064
• gnomAD v4: 1-119140344-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140344T>C , CM000663.2:g.119140344T>C	GRCh38
NC_000001.10:g.119682967T>C , CM000663.1:g.119682967T>C	GRCh37
NC_000001.9:g.119484490T>C	NCBI36
NG_050658.1:g.5445A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.90+211A>G MANE Select	ENSP00000235521.4:n.90+211A>G
ENST00000235521.4:c.90+211A>G	ENSP00000235521.4:n.90+211A>G
ENST00000369426.9:c.90+211A>G	ENSP00000358434.5:n.90+211A>G
ENST00000495746.5:n.100+211A>G
ENST00000497761.1:n.199A>G
NM_015836.3:c.90+211A>G	NP_056651.1:n.90+211A>G
NM_201263.2:c.90+211A>G	NP_957715.1:n.90+211A>G
XM_006710283.1:c.-269A>G	XP_006710346.1:n.-269A>G
XM_011540493.1:c.-141A>G	XP_011538795.1:n.-141A>G
XM_011540494.1:c.-65+211A>G	XP_011538796.1:n.-65+211A>G
XM_011540495.1:c.90+211A>G	XP_011538797.1:n.90+211A>G
XM_011540494.2:c.-65+211A>G	XP_011538796.1:n.-65+211A>G
XM_011540495.2:c.90+211A>G	XP_011538797.1:n.90+211A>G
XM_017000038.1:c.90+211A>G	XP_016855527.1:n.90+211A>G
XM_017000039.1:c.-141A>G	XP_016855528.1:n.-141A>G
XM_017000040.1:c.90+211A>G	XP_016855529.1:n.90+211A>G
XM_017000041.2:c.-269A>G	XP_016855530.1:n.-269A>G
XM_017000042.1:c.90+211A>G	XP_016855531.1:n.90+211A>G
XM_024449826.1:c.-141A>G	XP_024305594.1:n.-141A>G
XM_024449860.1:c.-269A>G	XP_024305628.1:n.-269A>G
XM_024449871.1:c.-269A>G	XP_024305639.1:n.-269A>G
NM_001378226.1:c.-65+211A>G	NP_001365155.1:n.-65+211A>G
NM_001378227.1:c.-141A>G	NP_001365156.1:n.-141A>G
NM_001378228.1:c.90+211A>G	NP_001365157.1:n.90+211A>G
NM_001378229.1:c.90+211A>G	NP_001365158.1:n.90+211A>G
NM_001378230.1:c.-269A>G	NP_001365159.1:n.-269A>G
NM_001378231.1:c.90+211A>G	NP_001365160.1:n.90+211A>G
NM_015836.4:c.90+211A>G MANE Select	NP_056651.1:n.90+211A>G