HGVS | Genome Assembly |
---|---|
NC_000006.12:g.111222750T>A , CM000668.2:g.111222750T>A | GRCh38 |
NC_000006.11:g.111543953T>A , CM000668.1:g.111543953T>A | GRCh37 |
NC_000006.10:g.111650646T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368851.10:c.*515T>A MANE Select | ENSP00000357844.4:n.*515T>A | |
ENST00000368850.4:c.*515T>A | ENSP00000357843.1:n.*515T>A | |
ENST00000368851.9:c.*515T>A | ENSP00000357844.4:n.*515T>A | |
NM_018593.4:c.*515T>A | NP_061063.2:n.*515T>A | |
XM_005266818.2:c.*469T>A | XP_005266875.1:n.*469T>A | |
XM_017010237.1:c.*515T>A | XP_016865726.1:n.*515T>A | |
XR_001743158.1:n.2345T>A | ||
NM_018593.5:c.*515T>A MANE Select | NP_061063.2:n.*515T>A |