Canonical Allele Identifier: CA401670108
Gene: TYMS HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.662193G>C (hg19) chr18:g.662193G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.662193G>C , CM000680.2:g.662193G>C GRCh38
NC_000018.9:g.662193G>C , CM000680.1:g.662193G>C GRCh37
NC_000018.8:g.652193G>C NCBI36
NG_028255.1:g.9590G>C , LRG_783:g.9590G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323274.15:c.327G>C MANE Select ENSP00000315644.10:p.Trp109Cys
ENST00000323224.7:c.327G>C ENSP00000314727.7:p.Trp109Cys
ENST00000323250.9:c.205+4246G>C ENSP00000314902.5:n.205+4246G>C
ENST00000323274.14:c.327G>C ENSP00000315644.10:p.Trp109Cys
ENST00000579128.1:n.405G>C
NM_001071.2:c.327G>C , LRG_783t1:c.327G>C NP_001062.1:p.Trp109Cys
NM_001071.3:c.327G>C NP_001062.1:p.Trp109Cys
NM_001354867.1:c.327G>C NP_001341796.1:p.Trp109Cys
NM_001354868.1:c.205+4246G>C NP_001341797.1:n.205+4246G>C
NM_001071.4:c.327G>C MANE Select NP_001062.1:p.Trp109Cys
NM_001354867.2:c.327G>C NP_001341796.1:p.Trp109Cys
NM_001354868.2:c.205+4246G>C NP_001341797.1:n.205+4246G>C
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