Canonical Allele Identifier: CA2263605814
Gene: NGFR HGNC NCBI
NGFR-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49508881A= , CM000679.2:g.49508881A= GRCh38
NC_000017.10:g.47586243A= , CM000679.1:g.47586243A= GRCh37
NC_000017.9:g.44941242A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000172229.8:c.569-1531A= (NGFR) MANE Select ENSP00000172229.3:n.569-1531A=
ENST00000172229.7:c.569-1531A= (NGFR) ENSP00000172229.3:n.569-1531A=
ENST00000504201.1:c.287-1531A= (NGFR) ENSP00000421731.1:n.287-1531A=
NM_002507.3:c.569-1531A= (NGFR) NP_002498.1:n.569-1531A=
NR_103773.1:n.377+2102T= (NGFR-AS1)
NM_002507.4:c.569-1531A= (NGFR) MANE Select NP_002498.1:n.569-1531A=
Search 100 bp 5'
Search 100 bp 3'