HGVS | Genome Assembly |
---|---|
NC_000023.11:g.106033593G>C , CM000685.2:g.106033593G>C | GRCh38 |
NC_000023.10:g.105277584G>C , CM000685.1:g.105277584G>C | GRCh37 |
NC_000023.9:g.105164240G>C | NCBI36 |
NG_021252.1:g.10135C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372563.2:c.1155C>G MANE Select | ENSP00000361644.1:p.Ile385Met | |
ENST00000327674.8:c.1155C>G | ENSP00000329374.4:p.Ile385Met | |
ENST00000372563.1:c.1155C>G | ENSP00000361644.1:p.Ile385Met | |
NM_000354.5:c.1155C>G | NP_000345.2:p.Ile385Met | |
XM_006724683.1:c.1185C>G | XP_006724746.1:p.Ile395Met | |
XM_005262180.4:c.*100C>G | XP_005262237.1:n.*100C>G | |
XM_006724683.2:c.1185C>G | XP_006724746.1:p.Ile395Met | |
NM_000354.6:c.1155C>G MANE Select | NP_000345.2:p.Ile385Met |