HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50816345T>G , CM000675.2:g.50816345T>G | GRCh38 |
NC_000013.10:g.51390481T>G , CM000675.1:g.51390481T>G | GRCh37 |
NC_000013.9:g.50288482T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651265.1:n.569+6848A>C (DLEU7) | ||
ENST00000651397.1:n.426+26843A>C (DLEU7) | ||
ENST00000400393.3:c.459+26843A>C (DLEU7) | ENSP00000420976.1:n.459+26843A>C | |
NM_198989.2:c.459+26843A>C (DLEU7) | NP_945340.2:n.459+26843A>C | |
NM_198989.3:c.459+26843A>C (DLEU7) | NP_945340.2:n.459+26843A>C | |
NR_046551.1:n.300-2176T>G (DLEU7-AS1) | ||
XM_011534973.1:c.459+26843A>C (DLEU7) | XP_011533275.1:n.459+26843A>C |