Canonical Allele Identifier: CA419368786

Linked Data

MyVariant Identifiers: chr1:g.110151237C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109608615C>G , CM000663.2:g.109608615C>G GRCh38
NC_000001.10:g.110151237C>G , CM000663.1:g.110151237C>G GRCh37
NC_000001.9:g.109952760C>G NCBI36
NG_009099.1:g.9469G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351050.8:c.461+16G>C (GNAT2) ENSP00000251337.3:n.461+16G>C
ENST00000679935.1:c.461+16G>C (GNAT2) MANE Select ENSP00000505083.1:n.461+16G>C
ENST00000351050.7:c.461+16G>C (GNAT2) ENSP00000251337.3:n.461+16G>C
ENST00000369851.5:c.*16293C>G (GNAI3) ENSP00000358867.4:n.*16293C>G
NM_005272.3:c.461+16G>C (GNAT2) NP_005263.1:n.461+16G>C
XM_011541264.1:c.461+16G>C (GNAT2) XP_011539566.1:n.461+16G>C
XM_011541265.1:c.461+16G>C (GNAT2) XP_011539567.1:n.461+16G>C
XM_011541266.1:c.461+16G>C (GNAT2) XP_011539568.1:n.461+16G>C
XM_011541264.2:c.461+16G>C (GNAT2) XP_011539566.1:n.461+16G>C
NM_001377295.1:c.461+16G>C (GNAT2) NP_001364224.1:n.461+16G>C
NM_005272.5:c.461+16G>C (GNAT2) NP_005263.1:n.461+16G>C
NM_001377295.2:c.461+16G>C (GNAT2) MANE Select NP_001364224.1:n.461+16G>C
NM_001379232.1:c.461+16G>C (GNAT2) NP_001366161.1:n.461+16G>C