Canonical Allele Identifier: CA1005651967

Linked Data

dbSNP Id: rs1649693389

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109608620G>T , CM000663.2:g.109608620G>T GRCh38
NC_000001.10:g.110151242G>T , CM000663.1:g.110151242G>T GRCh37
NC_000001.9:g.109952765G>T NCBI36
NG_009099.1:g.9464C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351050.8:c.461+11C>A (GNAT2) ENSP00000251337.3:n.461+11C>A
ENST00000679935.1:c.461+11C>A (GNAT2) MANE Select ENSP00000505083.1:n.461+11C>A
ENST00000351050.7:c.461+11C>A (GNAT2) ENSP00000251337.3:n.461+11C>A
ENST00000369851.5:c.*16298G>T (GNAI3) ENSP00000358867.4:n.*16298G>T
NM_005272.3:c.461+11C>A (GNAT2) NP_005263.1:n.461+11C>A
XM_011541264.1:c.461+11C>A (GNAT2) XP_011539566.1:n.461+11C>A
XM_011541265.1:c.461+11C>A (GNAT2) XP_011539567.1:n.461+11C>A
XM_011541266.1:c.461+11C>A (GNAT2) XP_011539568.1:n.461+11C>A
XM_011541264.2:c.461+11C>A (GNAT2) XP_011539566.1:n.461+11C>A
NM_001377295.1:c.461+11C>A (GNAT2) NP_001364224.1:n.461+11C>A
NM_005272.5:c.461+11C>A (GNAT2) NP_005263.1:n.461+11C>A
NM_001377295.2:c.461+11C>A (GNAT2) MANE Select NP_001364224.1:n.461+11C>A
NM_001379232.1:c.461+11C>A (GNAT2) NP_001366161.1:n.461+11C>A