Canonical Allele Identifier: CA2647274098

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115286803T>C , CM000663.2:g.115286803T>C GRCh38
NC_000001.10:g.115829424T>C , CM000663.1:g.115829424T>C GRCh37
NC_000001.9:g.115630947T>C NCBI36
NG_007944.1:g.56434A>G , LRG_260:g.56434A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369512.3:c.-8A>G (NGF) MANE Select ENSP00000358525.2:n.-8A>G
ENST00000675637.2:c.-8A>G (NGF) ENSP00000502831.1:n.-8A>G
ENST00000676038.2:c.-8A>G (NGF) ENSP00000502380.1:n.-8A>G
ENST00000679806.1:c.-8A>G (NGF) ENSP00000506492.1:n.-8A>G
ENST00000680116.1:c.-8A>G (NGF) ENSP00000505694.1:n.-8A>G
ENST00000680540.1:c.-8A>G (NGF) ENSP00000506569.1:n.-8A>G
ENST00000680752.1:c.-8A>G (NGF) ENSP00000505558.1:n.-8A>G
ENST00000681124.1:c.-420-59A>G (NGF) ENSP00000506364.1:n.-420-59A>G
ENST00000369512.2:c.-8A>G (NGF) ENSP00000358525.2:n.-8A>G
NM_002506.2:c.-8A>G , LRG_260t1:c.-8A>G (NGF) NP_002497.2:n.-8A>G
XM_006710663.2:c.-8A>G (NGF) XP_006710726.1:n.-8A>G
XM_006710665.2:c.-8A>G (NGF) XP_006710728.1:n.-8A>G
XM_011541518.1:c.158A>G (NGF) XP_011539820.1:p.His53Arg
NR_157569.1:n.207+3563T>C (NGF-AS1)
XM_006710663.3:c.-8A>G (NGF) XP_006710726.1:n.-8A>G
XM_011541518.2:c.158A>G (NGF) XP_011539820.1:p.His53Arg
NM_002506.3:c.-8A>G (NGF) MANE Select NP_002497.2:n.-8A>G