Canonical Allele Identifier: CA764607646

Gene: ATIC

Linked Data

• dbSNP Id: rs12471482
• MyVariant Identifiers: chr2:g.216209303T>A (hg19) ; chr2:g.215344580T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.215344580T>A , CM000664.2:g.215344580T>A	GRCh38
NC_000002.11:g.216209303T>A , CM000664.1:g.216209303T>A	GRCh37
NC_000002.10:g.215917548T>A	NCBI36
NG_013002.1:g.37625T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236959.14:c.1228-199T>A MANE Select	ENSP00000236959.9:n.1228-199T>A
ENST00000236959.13:c.1228-199T>A	ENSP00000236959.9:n.1228-199T>A
ENST00000426233.1:c.233-199T>A
ENST00000435675.5:c.1225-199T>A	ENSP00000415935.1:n.1225-199T>A
ENST00000443953.5:c.*1325-199T>A	ENSP00000406792.1:n.*1325-199T>A
ENST00000446622.5:n.308-199T>A
ENST00000459796.1:n.39-199T>A
ENST00000467388.1:n.140-199T>A
ENST00000479093.5:n.143-199T>A
NM_004044.6:c.1228-199T>A	NP_004035.2:n.1228-199T>A
XM_017004187.2:c.1228-199T>A	XP_016859676.1:n.1228-199T>A
XM_024452919.1:c.1051-199T>A	XP_024308687.1:n.1051-199T>A
NM_004044.7:c.1228-199T>A MANE Select	NP_004035.2:n.1228-199T>A