HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978092C>T , CM000667.2:g.149978092C>T | GRCh38 |
NC_000005.9:g.149357655C>T , CM000667.1:g.149357655C>T | GRCh37 |
NC_000005.8:g.149337848C>T | NCBI36 |
NG_007147.2:g.19210C>T , LRG_684:g.19210C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.672C>T | ||
ENST00000286298.5:c.440C>T MANE Select | ENSP00000286298.4:p.Ala147Val | |
ENST00000286298.4:c.440C>T | ENSP00000286298.4:p.Ala147Val | |
ENST00000503336.1:c.113C>T | ENSP00000426053.1:p.Ala38Val | |
NM_000112.3:c.440C>T , LRG_684t1:c.440C>T | NP_000103.2:p.Ala147Val | |
XM_017009191.2:c.440C>T | XP_016864680.1:p.Ala147Val | |
NM_000112.4:c.440C>T MANE Select | NP_000103.2:p.Ala147Val |