Canonical Allele Identifier: CA13630500
Gene: GLT8D2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2629751

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.104028030A>G , CM000674.2:g.104028030A>G GRCh38
NC_000012.11:g.104421808A>G , CM000674.1:g.104421808A>G GRCh37
NC_000012.10:g.102945938A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001316967.1:c.-28-8354T>C VV NP_001303896.1:p.=
NM_031302.3:c.-163-6539T>C VV NP_112592.1:p.=
NM_031302.4:c.-163-6539T>C VV NP_112592.1:p.=
XM_011538793.1:c.-163-6539T>C XP_011537095.1:p.=
XM_011538794.1:c.-164+1666T>C XP_011537096.1:p.=
XM_011538793.3:c.-163-6539T>C XP_011537095.1:p.=
XM_017019999.1:c.-163-6539T>C XP_016875488.1:p.=
ENST00000360814.8:c.-163-6539T>C ENSP00000354053.4:p.=
ENST00000546436.5:c.-29+1666T>C ENSP00000449750.1:p.=
ENST00000546851.1:c.-72+21393T>C ENSP00000446810.1:p.=
ENST00000547583.1:c.-163-6539T>C ENSP00000448065.1:p.=
ENST00000548660.5:c.-28-8354T>C ENSP00000447450.1:p.=
ENST00000550816.1:n.128-8354T>C