HGVS | Genome Assembly |
---|---|
NC_000017.11:g.49508920T>C , CM000679.2:g.49508920T>C | GRCh38 |
NC_000017.10:g.47586282T>C , CM000679.1:g.47586282T>C | GRCh37 |
NC_000017.9:g.44941281T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000172229.8:c.569-1492T>C (NGFR) MANE Select | ENSP00000172229.3:n.569-1492T>C | |
ENST00000172229.7:c.569-1492T>C (NGFR) | ENSP00000172229.3:n.569-1492T>C | |
ENST00000504201.1:c.287-1492T>C (NGFR) | ENSP00000421731.1:n.287-1492T>C | |
NM_002507.3:c.569-1492T>C (NGFR) | NP_002498.1:n.569-1492T>C | |
NR_103773.1:n.377+2063A>G (NGFR-AS1) | ||
NM_002507.4:c.569-1492T>C (NGFR) MANE Select | NP_002498.1:n.569-1492T>C |