Canonical Allele Identifier: CA14506233
Gene: TYMS HGNC NCBI

Linked Data

dbSNP Id: rs502396
gnomAD v2: 18-659236-C-T
gnomAD v3: 18-659236-C-T
gnomAD v4: 18-659236-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.659236C>T , CM000680.2:g.659236C>T GRCh38
NC_000018.9:g.659236C>T , CM000680.1:g.659236C>T GRCh37
NC_000018.8:g.649236C>T NCBI36
NG_028255.1:g.6633C>T , LRG_783:g.6633C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323274.15:c.206-405C>T MANE Select ENSP00000315644.10:n.206-405C>T
ENST00000323224.7:c.206-405C>T ENSP00000314727.7:n.206-405C>T
ENST00000323250.9:c.205+1289C>T ENSP00000314902.5:n.205+1289C>T
ENST00000323274.14:c.206-405C>T ENSP00000315644.10:n.206-405C>T
ENST00000579128.1:n.284-405C>T
ENST00000584122.1:n.486-405C>T
NM_001071.2:c.206-405C>T , LRG_783t1:c.206-405C>T NP_001062.1:n.206-405C>T
NM_001071.3:c.206-405C>T NP_001062.1:n.206-405C>T
NM_001354867.1:c.206-405C>T NP_001341796.1:n.206-405C>T
NM_001354868.1:c.205+1289C>T NP_001341797.1:n.205+1289C>T
NM_001071.4:c.206-405C>T MANE Select NP_001062.1:n.206-405C>T
NM_001354867.2:c.206-405C>T NP_001341796.1:n.206-405C>T
NM_001354868.2:c.205+1289C>T NP_001341797.1:n.205+1289C>T