HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11965533A>T , CM000663.2:g.11965533A>T | GRCh38 |
NC_000001.10:g.12025590A>T , CM000663.1:g.12025590A>T | GRCh37 |
NC_000001.9:g.11948177A>T | NCBI36 |
NG_008159.1:g.35845A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000196061.5:c.1524A>T MANE Select | ENSP00000196061.4:p.Leu508= | |
ENST00000196061.4:c.1524A>T | ENSP00000196061.4:p.Leu508= | |
ENST00000470133.1:n.138A>T | ||
ENST00000491536.5:n.152A>T | ||
NM_000302.3:c.1524A>T | NP_000293.2:p.Leu508= | |
NM_001316320.1:c.1665A>T | NP_001303249.1:p.Leu555= | |
XM_011541594.1:c.1605A>T | XP_011539896.1:p.Leu535= | |
XM_024447707.1:c.858A>T | XP_024303475.1:p.Leu286= | |
NM_000302.4:c.1524A>T MANE Select | NP_000293.2:p.Leu508= | |
NM_001316320.2:c.1665A>T | NP_001303249.1:p.Leu555= |