HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50816475A>G , CM000675.2:g.50816475A>G | GRCh38 |
NC_000013.10:g.51390611A>G , CM000675.1:g.51390611A>G | GRCh37 |
NC_000013.9:g.50288612A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651265.1:n.569+6718T>C (DLEU7) | ||
ENST00000651397.1:n.426+26713T>C (DLEU7) | ||
ENST00000400393.3:c.459+26713T>C (DLEU7) | ENSP00000420976.1:n.459+26713T>C | |
NM_198989.2:c.459+26713T>C (DLEU7) | NP_945340.2:n.459+26713T>C | |
NM_198989.3:c.459+26713T>C (DLEU7) | NP_945340.2:n.459+26713T>C | |
NR_046551.1:n.300-2046A>G (DLEU7-AS1) | ||
XM_011534973.1:c.459+26713T>C (DLEU7) | XP_011533275.1:n.459+26713T>C |