HGVS | Genome Assembly |
---|---|
NC_000010.11:g.49474234G>A , CM000672.2:g.49474234G>A | GRCh38 |
NC_000010.10:g.50682280G>A , CM000672.1:g.50682280G>A | GRCh37 |
NC_000010.9:g.50352286G>A | NCBI36 |
NG_009442.1:g.69868C>T , LRG_465:g.69868C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355832.10:c.2391C>T MANE Select | ENSP00000348089.5:p.Ser797= | |
ENST00000681632.1:n.2469C>T | ||
ENST00000681659.1:c.2232C>T | ENSP00000505631.1:p.Ser744= | |
ENST00000355832.9:c.2391C>T | ENSP00000348089.5:p.Ser797= | |
ENST00000623073.3:c.*687C>T | ENSP00000485650.1:n.*687C>T | |
ENST00000623115.3:c.501C>T | ENSP00000485321.1:p.Ser167= | |
ENST00000624341.3:c.223C>T | ||
NM_000124.3:c.2391C>T | NP_000115.1:p.Ser797= | |
NM_001346440.1:c.2391C>T | NP_001333369.1:p.Ser797= | |
NM_000124.4:c.2391C>T MANE Select | NP_000115.1:p.Ser797= | |
NM_001346440.2:c.2391C>T | NP_001333369.1:p.Ser797= |