Canonical Allele Identifier: CA2263605811
Gene: NGFR HGNC NCBI
NGFR-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49508868C= , CM000679.2:g.49508868C= GRCh38
NC_000017.10:g.47586230C= , CM000679.1:g.47586230C= GRCh37
NC_000017.9:g.44941229C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000172229.8:c.569-1544C= (NGFR) MANE Select ENSP00000172229.3:n.569-1544C=
ENST00000172229.7:c.569-1544C= (NGFR) ENSP00000172229.3:n.569-1544C=
ENST00000504201.1:c.287-1544C= (NGFR) ENSP00000421731.1:n.287-1544C=
NM_002507.3:c.569-1544C= (NGFR) NP_002498.1:n.569-1544C=
NR_103773.1:n.377+2115G= (NGFR-AS1)
NM_002507.4:c.569-1544C= (NGFR) MANE Select NP_002498.1:n.569-1544C=
Search 100 bp 5'
Search 100 bp 3'