Canonical Allele Identifier: CA2263605816
Gene: NGFR HGNC NCBI
NGFR-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49508888G= , CM000679.2:g.49508888G= GRCh38
NC_000017.10:g.47586250G= , CM000679.1:g.47586250G= GRCh37
NC_000017.9:g.44941249G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000172229.8:c.569-1524G= (NGFR) MANE Select ENSP00000172229.3:n.569-1524G=
ENST00000172229.7:c.569-1524G= (NGFR) ENSP00000172229.3:n.569-1524G=
ENST00000504201.1:c.287-1524G= (NGFR) ENSP00000421731.1:n.287-1524G=
NM_002507.3:c.569-1524G= (NGFR) NP_002498.1:n.569-1524G=
NR_103773.1:n.377+2095C= (NGFR-AS1)
NM_002507.4:c.569-1524G= (NGFR) MANE Select NP_002498.1:n.569-1524G=
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