Canonical Allele Identifier: CA291472222
Gene: NGFR HGNC NCBI
NGFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs552625119
gnomAD v3: 17-49508881-A-C
gnomAD v4: 17-49508881-A-C
MyVariant Identifiers: chr17:g.47586243A>C (hg19) chr17:g.49508881A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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