HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219418550C= , CM000664.2:g.219418550C= | GRCh38 |
NC_000002.11:g.220283272C= , CM000664.1:g.220283272C= | GRCh37 |
NC_000002.10:g.219991516C= | NCBI36 |
NG_008043.1:g.5174C= , LRG_380:g.5174C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373960.4:c.88C= MANE Select | ENSP00000363071.3:p.Leu30= | |
ENST00000373960.3:c.88C= | ENSP00000363071.3:p.Leu30= | |
NM_001927.3:c.88C= , LRG_380t1:c.88C= | NP_001918.3:p.Leu30= | |
NM_001927.4:c.88C= MANE Select | NP_001918.3:p.Leu30= | |
NM_001382708.1:c.88C= | NP_001369637.1:p.Leu30= | |
NM_001382709.1:c.88C= | NP_001369638.1:p.Leu30= | |
NM_001382710.1:c.88C= | NP_001369639.1:p.Leu30= | |
NM_001382711.1:c.88C= | NP_001369640.1:p.Leu30= | |
NM_001382712.1:c.88C= | NP_001369641.1:p.Leu30= | |
NM_001382713.1:c.88C= | NP_001369642.1:p.Leu30= |