Canonical Allele Identifier: CA170993
Gene: MTR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 138289
dbSNP Id: rs1805087

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.236885200A>G , CM000663.2:g.236885200A>G GRCh38
NC_000001.9:g.235115123A>G NCBI36
NC_000001.10:g.237048500A>G , CM000663.1:g.237048500A>G GRCh37
NG_008959.1:g.94920A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366576.3:n.1418A>G ENSP00000355535.3:p.Asp473Gly
ENST00000366577.9:c.2756A>G ENSP00000355536.5:p.Asp919Gly
ENST00000535889.5:c.2603A>G ENSP00000441845.1:p.Asp868Gly
NM_000254.2:c.2756A>G VV NP_000245.2:p.Asp919Gly
NM_001291939.1:c.2603A>G VV NP_001278868.1:p.Asp868Gly
NM_001291940.1:c.1535A>G VV NP_001278869.1:p.Asp512Gly
XM_005273141.3:c.2753A>G XP_005273198.1:p.Asp918Gly
XM_006711769.2:c.2756A>G XP_006711832.1:p.Asp919Gly
XM_006711770.1:c.1820A>G XP_006711833.1:p.Asp607Gly
XM_011544193.1:c.2567A>G XP_011542495.1:p.Asp856Gly
XM_011544194.1:c.2924A>G XP_011542496.1:p.Asp975Gly