Canonical Allele Identifier: CA1190555182

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115338434G>T , CM000663.2:g.115338434G>T GRCh38
NC_000001.10:g.115881055G>T , CM000663.1:g.115881055G>T GRCh37
NC_000001.9:g.115682578G>T NCBI36
NG_007944.1:g.4803C>A , LRG_260:g.4803C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679806.1:c.-137+174C>A (NGF) ENSP00000506492.1:n.-137+174C>A
ENST00000680752.1:c.-206C>A (NGF) ENSP00000505558.1:n.-206C>A
NR_157569.1:n.208-27236G>T (NGF-AS1)