Canonical Allele Identifier: CA2841765497

Gene: NGFR NGFR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49508847T>C , CM000679.2:g.49508847T>C	GRCh38
NC_000017.10:g.47586209T>C , CM000679.1:g.47586209T>C	GRCh37
NC_000017.9:g.44941208T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000172229.8:c.569-1565T>C (NGFR) MANE Select	ENSP00000172229.3:n.569-1565T>C
ENST00000172229.7:c.569-1565T>C (NGFR)	ENSP00000172229.3:n.569-1565T>C
ENST00000504201.1:c.287-1565T>C (NGFR)	ENSP00000421731.1:n.287-1565T>C
NM_002507.3:c.569-1565T>C (NGFR)	NP_002498.1:n.569-1565T>C
NR_103773.1:n.377+2136A>G (NGFR-AS1)
NM_002507.4:c.569-1565T>C (NGFR) MANE Select	NP_002498.1:n.569-1565T>C