Canonical Allele Identifier: CA2696633485

Linked Data

dbSNP Id: rs2101126607

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109608609C>A , CM000663.2:g.109608609C>A GRCh38
NC_000001.10:g.110151231C>A , CM000663.1:g.110151231C>A GRCh37
NC_000001.9:g.109952754C>A NCBI36
NG_009099.1:g.9475G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351050.8:c.461+22G>T (GNAT2) ENSP00000251337.3:n.461+22G>T
ENST00000679935.1:c.461+22G>T (GNAT2) MANE Select ENSP00000505083.1:n.461+22G>T
ENST00000351050.7:c.461+22G>T (GNAT2) ENSP00000251337.3:n.461+22G>T
ENST00000369851.5:c.*16287C>A (GNAI3) ENSP00000358867.4:n.*16287C>A
NM_005272.3:c.461+22G>T (GNAT2) NP_005263.1:n.461+22G>T
XM_011541264.1:c.461+22G>T (GNAT2) XP_011539566.1:n.461+22G>T
XM_011541265.1:c.461+22G>T (GNAT2) XP_011539567.1:n.461+22G>T
XM_011541266.1:c.461+22G>T (GNAT2) XP_011539568.1:n.461+22G>T
XM_011541264.2:c.461+22G>T (GNAT2) XP_011539566.1:n.461+22G>T
NM_001377295.1:c.461+22G>T (GNAT2) NP_001364224.1:n.461+22G>T
NM_005272.5:c.461+22G>T (GNAT2) NP_005263.1:n.461+22G>T
NM_001377295.2:c.461+22G>T (GNAT2) MANE Select NP_001364224.1:n.461+22G>T
NM_001379232.1:c.461+22G>T (GNAT2) NP_001366161.1:n.461+22G>T