HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110910998A>G , CM000674.2:g.110910998A>G | GRCh38 |
NC_000012.11:g.111348802A>G , CM000674.1:g.111348802A>G | GRCh37 |
NC_000012.10:g.109833185A>G | NCBI36 |
NG_007554.1:g.14580T>C , LRG_393:g.14580T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.*79T>C MANE Select | ENSP00000228841.8:n.*79T>C | |
ENST00000663220.1:c.*79T>C | ENSP00000499568.1:n.*79T>C | |
ENST00000228841.12:c.*79T>C | ENSP00000228841.7:n.*79T>C | |
ENST00000548438.1:c.*79T>C | ENSP00000447154.1:n.*79T>C | |
NM_000432.3:c.*79T>C , LRG_393t1:c.*79T>C | NP_000423.2:n.*79T>C | |
NM_000432.4:c.*79T>C MANE Select | NP_000423.2:n.*79T>C |