HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99845688T= , CM000672.2:g.99845688T= | GRCh38 |
NC_000010.10:g.101605445T= , CM000672.1:g.101605445T= | GRCh37 |
NC_000010.9:g.101595435T= | NCBI36 |
NG_011798.1:g.67983T= | |
NG_011798.2:g.68091T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647814.1:c.4052T= MANE Select | ENSP00000497274.1:p.Leu1351= | |
ENST00000649459.1:n.400T= | ||
ENST00000370449.8:c.4052T= | ENSP00000359478.4:p.Leu1351= | |
NM_000392.4:c.4052T= | NP_000383.1:p.Leu1351= | |
XM_006717630.2:c.3356T= | XP_006717693.1:p.Leu1119= | |
XR_945604.1:n.4182T= | ||
XR_945605.1:n.4116T= | ||
NM_000392.5:c.4052T= MANE Select | NP_000383.2:p.Leu1351= | |
XM_006717630.3:c.3356T= | XP_006717693.1:p.Leu1119= | |
XR_945604.3:n.4236T= | ||
XR_945605.3:n.4168T= |