Canonical Allele Identifier: CA401670216

Gene: TYMS

Linked Data

• MyVariant Identifiers: chr18:g.662223C>G (hg19) ; chr18:g.662223C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.662223C>G , CM000680.2:g.662223C>G	GRCh38
NC_000018.9:g.662223C>G , CM000680.1:g.662223C>G	GRCh37
NC_000018.8:g.652223C>G	NCBI36
NG_028255.1:g.9620C>G , LRG_783:g.9620C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323274.15:c.357C>G MANE Select	ENSP00000315644.10:p.Asp119Glu
ENST00000323224.7:c.357C>G	ENSP00000314727.7:p.Asp119Glu
ENST00000323250.9:c.205+4276C>G	ENSP00000314902.5:n.205+4276C>G
ENST00000323274.14:c.357C>G	ENSP00000315644.10:p.Asp119Glu
ENST00000579128.1:n.435C>G
NM_001071.2:c.357C>G , LRG_783t1:c.357C>G	NP_001062.1:p.Asp119Glu
NM_001071.3:c.357C>G	NP_001062.1:p.Asp119Glu
NM_001354867.1:c.357C>G	NP_001341796.1:p.Asp119Glu
NM_001354868.1:c.205+4276C>G	NP_001341797.1:n.205+4276C>G
NM_001071.4:c.357C>G MANE Select	NP_001062.1:p.Asp119Glu
NM_001354867.2:c.357C>G	NP_001341796.1:p.Asp119Glu
NM_001354868.2:c.205+4276C>G	NP_001341797.1:n.205+4276C>G