HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997021G>A , CM000685.2:g.154997021G>A | GRCh38 |
NC_000023.10:g.154225296G>A , CM000685.1:g.154225296G>A | GRCh37 |
NC_000023.9:g.153878490G>A | NCBI36 |
NG_011403.1:g.30703C>T | |
NG_011403.2:g.30703C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.340C>T MANE Select | ENSP00000353393.4:p.Pro114Ser | |
ENST00000647125.1:c.*126C>T | ENSP00000496062.1:n.*126C>T | |
ENST00000360256.8:c.340C>T | ENSP00000353393.4:p.Pro114Ser | |
ENST00000423959.5:c.235C>T | ENSP00000409446.1:p.Pro79Ser | |
ENST00000453950.1:c.322C>T | ENSP00000389153.1:p.Pro108Ser | |
NM_000132.3:c.340C>T | NP_000123.1:p.Pro114Ser | |
XM_011531126.1:c.235C>T | XP_011529428.1:p.Pro79Ser | |
NM_000132.4:c.340C>T MANE Select | NP_000123.1:p.Pro114Ser |