Canonical Allele Identifier: CA118170
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 6368
dbSNP Id: rs121908920

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166311573T>C , CM000664.2:g.166311573T>C GRCh38
NC_000002.11:g.167168083T>C , CM000664.1:g.167168083T>C GRCh37
NC_000002.10:g.166876329T>C NCBI36
NG_012798.1:g.69415A>G , LRG_369:g.69415A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.184A>G ENSP00000304748.7:p.Ile62Val
ENST00000409435.6:n.184A>G ENSP00000386330.2:p.Ile62Val
ENST00000452182.2:c.184A>G ENSP00000393141.2:p.Ile62Val
ENST00000454569.6:c.184A>G ENSP00000413212.2:p.Ile62Val
ENST00000472119.2:n.539A>G
ENST00000642356.2:c.184A>G MANE Select ENSP00000495601.1:p.Ile62Val
ENST00000644316.1:n.184A>G ENSP00000493939.1:p.Ile62Val
ENST00000645907.1:c.184A>G ENSP00000495983.1:p.Ile62Val
ENST00000667991.1:c.184A>G ENSP00000499663.1:p.Ile62Val
ENST00000303354.10:c.184A>G ENSP00000304748.7:p.Ile62Val
ENST00000409435.5:n.184A>G ENSP00000386330.1:p.Ile62Val
ENST00000409672.5:c.184A>G ENSP00000386306.1:p.Ile62Val
NM_002977.3:c.184A>G , LRG_369t1:c.184A>G NP_002968.1:p.Ile62Val
XM_005246757.1:c.184A>G XP_005246814.1:p.Ile62Val
XM_011511616.1:c.184A>G XP_011509918.1:p.Ile62Val
XM_011511617.1:c.184A>G XP_011509919.1:p.Ile62Val
XM_011511618.1:c.184A>G XP_011509920.1:p.Ile62Val
XM_011511619.1:c.184A>G XP_011509921.1:p.Ile62Val
NM_001365536.1:c.184A>G MANE Select NP_001352465.1:p.Ile62Val
XM_011511616.3:c.184A>G XP_011509918.1:p.Ile62Val
XM_011511617.2:c.184A>G XP_011509919.1:p.Ile62Val
XM_011511618.2:c.184A>G XP_011509920.1:p.Ile62Val
XM_011511619.2:c.184A>G XP_011509921.1:p.Ile62Val
XM_017004668.1:c.-218A>G XP_016860157.1:p.=
XR_001738886.1:n.498A>G