HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57764144A>C , CM000674.2:g.57764144A>C | GRCh38 |
NC_000012.11:g.58157927A>C , CM000674.1:g.58157927A>C | GRCh37 |
NC_000012.10:g.56444194A>C | NCBI36 |
NG_007076.1:g.8050T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000713544.1:c.1250T>G | ENSP00000518840.1:p.Val417Gly | |
ENST00000713545.1:c.*174T>G | ENSP00000518841.1:n.*174T>G | |
ENST00000228606.9:c.1169T>G MANE Select | ENSP00000228606.4:p.Val390Gly | |
ENST00000228606.8:c.1169T>G | ENSP00000228606.4:p.Val390Gly | |
ENST00000546567.5:c.464T>G | ENSP00000449472.1:p.Val155Gly | |
ENST00000547344.5:n.1308T>G | ||
NM_000785.3:c.1169T>G | NP_000776.1:p.Val390Gly | |
NM_000785.4:c.1169T>G MANE Select | NP_000776.1:p.Val390Gly |