Canonical Allele Identifier: CA1023067

Linked Data

ClinVar Variation Id: 291993
dbSNP Id: rs6330

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115286692G>A , CM000663.2:g.115286692G>A GRCh38
NC_000001.10:g.115829313G>A , CM000663.1:g.115829313G>A GRCh37
NC_000001.9:g.115630836G>A NCBI36
NG_007944.1:g.56545C>T , LRG_260:g.56545C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369512.3:c.104C>T (NGF) MANE Select ENSP00000358525.2:p.Ala35Val
ENST00000675637.2:c.104C>T ENSP00000502831.1:p.Ala35Val
ENST00000676038.2:c.104C>T ENSP00000502380.1:p.Ala35Val
ENST00000679806.1:c.104C>T ENSP00000506492.1:p.Ala35Val
ENST00000680116.1:c.104C>T ENSP00000505694.1:p.Ala35Val
ENST00000680540.1:c.104C>T ENSP00000506569.1:p.Ala35Val
ENST00000680752.1:c.104C>T ENSP00000505558.1:p.Ala35Val
ENST00000681124.1:c.-368C>T ENSP00000506364.1:p.=
ENST00000369512.2:c.104C>T ENSP00000358525.2:p.Ala35Val
NM_002506.2:c.104C>T , LRG_260t1:c.104C>T (NGF) NP_002497.2:p.Ala35Val
XM_006710663.2:c.104C>T (NGF) XP_006710726.1:p.Ala35Val
XM_006710665.2:c.104C>T (NGF) XP_006710728.1:p.Ala35Val
XM_011541518.1:c.269C>T (NGF) XP_011539820.1:p.Ala90Val
NR_157569.1:n.207+3452G>A (NGF-AS1)
XM_006710663.3:c.104C>T (NGF) XP_006710726.1:p.Ala35Val
XM_011541518.2:c.269C>T (NGF) XP_011539820.1:p.Ala90Val
NM_002506.3:c.104C>T (NGF) MANE Select NP_002497.2:p.Ala35Val