Canonical Allele Identifier: CA291472221
Gene: NGFR HGNC NCBI
NGFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs532121890
gnomAD v3: 17-49508875-G-T
gnomAD v4: 17-49508875-G-T
MyVariant Identifiers: chr17:g.47586237G>T (hg19) chr17:g.49508875G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49508875G>T , CM000679.2:g.49508875G>T GRCh38
NC_000017.10:g.47586237G>T , CM000679.1:g.47586237G>T GRCh37
NC_000017.9:g.44941236G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000172229.8:c.569-1537G>T (NGFR) MANE Select ENSP00000172229.3:n.569-1537G>T
ENST00000172229.7:c.569-1537G>T (NGFR) ENSP00000172229.3:n.569-1537G>T
ENST00000504201.1:c.287-1537G>T (NGFR) ENSP00000421731.1:n.287-1537G>T
NM_002507.3:c.569-1537G>T (NGFR) NP_002498.1:n.569-1537G>T
NR_103773.1:n.377+2108C>A (NGFR-AS1)
NM_002507.4:c.569-1537G>T (NGFR) MANE Select NP_002498.1:n.569-1537G>T
Search 100 bp 5'
Search 100 bp 3'