Canonical Allele Identifier: CA59812603
Gene: SCN9A HGNC NCBI

Linked Data

dbSNP Id: rs4438497

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.166320849T>C , CM000664.2:g.166320849T>C GRCh38
NC_000002.11:g.167177359T>C , CM000664.1:g.167177359T>C GRCh37
NC_000002.10:g.166885605T>C NCBI36
NG_012798.1:g.60139A>G , LRG_369:g.60139A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303354.11:c.-50-9043A>G ENSP00000304748.7:p.=
ENST00000452182.2:c.-51+590A>G ENSP00000393141.2:p.=
ENST00000454569.6:c.-50-9043A>G ENSP00000413212.2:p.=
ENST00000472119.2:n.306-9043A>G
ENST00000642356.2:c.-50-9043A>G MANE Select ENSP00000495601.1:p.=
ENST00000645907.1:c.-50-9043A>G ENSP00000495983.1:p.=
ENST00000303354.10:c.-50-9043A>G ENSP00000304748.7:p.=
ENST00000409672.5:c.-50-9043A>G ENSP00000386306.1:p.=
NM_002977.3:c.-50-9043A>G , LRG_369t1:c.-50-9043A>G NP_002968.1:p.=
XM_005246757.1:c.-50-9043A>G XP_005246814.1:p.=
XM_011511616.1:c.-50-9043A>G XP_011509918.1:p.=
XM_011511617.1:c.-50-9043A>G XP_011509919.1:p.=
XM_011511618.1:c.-50-9043A>G XP_011509920.1:p.=
XM_011511619.1:c.-50-9043A>G XP_011509921.1:p.=
NM_001365536.1:c.-50-9043A>G MANE Select NP_001352465.1:p.=
XM_011511616.3:c.-50-9043A>G XP_011509918.1:p.=
XM_011511617.2:c.-50-9043A>G XP_011509919.1:p.=
XM_011511618.2:c.-50-9043A>G XP_011509920.1:p.=
XM_011511619.2:c.-50-9043A>G XP_011509921.1:p.=
XR_001738886.1:n.265-9043A>G