Canonical Allele Identifier: CA401669837

Gene: TYMS

Linked Data

• MyVariant Identifiers: chr18:g.662146G>C (hg19) ; chr18:g.662146G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.662146G>C , CM000680.2:g.662146G>C	GRCh38
NC_000018.9:g.662146G>C , CM000680.1:g.662146G>C	GRCh37
NC_000018.8:g.652146G>C	NCBI36
NG_028255.1:g.9543G>C , LRG_783:g.9543G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.280G>C MANE Select	ENSP00000315644.10:p.Gly94Arg
ENST00000323224.7:c.280G>C	ENSP00000314727.7:p.Gly94Arg
ENST00000323250.9:c.205+4199G>C	ENSP00000314902.5:n.205+4199G>C
ENST00000323274.14:c.280G>C	ENSP00000315644.10:p.Gly94Arg
ENST00000579128.1:n.358G>C
NM_001071.2:c.280G>C , LRG_783t1:c.280G>C	NP_001062.1:p.Gly94Arg
NM_001071.3:c.280G>C	NP_001062.1:p.Gly94Arg
NM_001354867.1:c.280G>C	NP_001341796.1:p.Gly94Arg
NM_001354868.1:c.205+4199G>C	NP_001341797.1:n.205+4199G>C
NM_001071.4:c.280G>C MANE Select	NP_001062.1:p.Gly94Arg
NM_001354867.2:c.280G>C	NP_001341796.1:p.Gly94Arg
NM_001354868.2:c.205+4199G>C	NP_001341797.1:n.205+4199G>C