HGVS | Genome Assembly |
---|---|
NC_000018.10:g.7042165A>C , CM000680.2:g.7042165A>C | GRCh38 |
NC_000018.9:g.7042164A>C , CM000680.1:g.7042164A>C | GRCh37 |
NC_000018.8:g.7032164A>C | NCBI36 |
NG_034251.1:g.80650T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000389658.4:c.1241T>G MANE Select | ENSP00000374309.3:p.Leu414Arg | |
ENST00000389658.3:c.1241T>G | ENSP00000374309.3:p.Leu414Arg | |
ENST00000579014.5:n.2256T>G | ||
NM_005559.3:c.1241T>G | NP_005550.2:p.Leu414Arg | |
XM_011525655.1:c.1241T>G | XP_011523957.1:p.Leu414Arg | |
XM_011525657.1:c.1241T>G | XP_011523959.1:p.Leu414Arg | |
XM_011525655.2:c.1241T>G | XP_011523957.1:p.Leu414Arg | |
NM_005559.4:c.1241T>G MANE Select | NP_005550.2:p.Leu414Arg |