Canonical Allele Identifier: CA350473351
Gene: ATIC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.216190019A>T (hg19) chr2:g.215325296A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325296A>T , CM000664.2:g.215325296A>T GRCh38
NC_000002.11:g.216190019A>T , CM000664.1:g.216190019A>T GRCh37
NC_000002.10:g.215898264A>T NCBI36
NG_013002.1:g.18341A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.346A>T MANE Select ENSP00000236959.9:p.Thr116Ser
ENST00000236959.13:c.346A>T ENSP00000236959.9:p.Thr116Ser
ENST00000413174.1:c.169A>T ENSP00000402393.1:p.Thr57Ser
ENST00000427397.5:c.*396A>T ENSP00000394317.1:n.*396A>T
ENST00000435675.5:c.343A>T ENSP00000415935.1:p.Thr115Ser
ENST00000443953.5:c.*443A>T ENSP00000406792.1:n.*443A>T
ENST00000444305.5:c.*24A>T ENSP00000388675.1:n.*24A>T
ENST00000488712.5:n.558A>T
NM_004044.6:c.346A>T NP_004035.2:p.Thr116Ser
XM_017004187.2:c.346A>T XP_016859676.1:p.Thr116Ser
XM_024452919.1:c.169A>T XP_024308687.1:p.Thr57Ser
NM_004044.7:c.346A>T MANE Select NP_004035.2:p.Thr116Ser
Search 100 bp 5'
Search 100 bp 3'