HGVS | Genome Assembly |
---|---|
NC_000021.9:g.43169154C>T , CM000683.2:g.43169154C>T | GRCh38 |
NG_009823.1:g.5124C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291554.6:c.55C>T MANE Select | ENSP00000291554.2:p.Pro19Ser | |
ENST00000482775.1:n.68C>T | ||
NM_000394.3:c.55C>T | NP_000385.1:p.Pro19Ser | |
XR_001755073.1:n.647+1883G>A | ||
NM_000394.4:c.55C>T MANE Select | NP_000385.1:p.Pro19Ser |