HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40292603G= , CM000663.2:g.40292603G= | GRCh38 |
NC_000001.10:g.40758275G= , CM000663.1:g.40758275G= | GRCh37 |
NC_000001.9:g.40530862G= | NCBI36 |
NG_008695.1:g.39543G= , LRG_212:g.39543G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372759.4:c.1362G= MANE Select | ENSP00000361845.3:p.Met454= | |
ENST00000674703.1:c.*1203G= | ENSP00000501674.1:n.*1203G= | |
ENST00000675754.1:c.*1104G= | ENSP00000502555.1:n.*1104G= | |
ENST00000675937.1:c.*607G= | ENSP00000502683.1:n.*607G= | |
ENST00000372759.3:c.1362G= | ENSP00000361845.3:p.Met454= | |
ENST00000474142.1:n.512G= | ||
NM_005857.4:c.1362G= | NP_005848.2:p.Met454= | |
XM_011540486.1:c.1113G= | XP_011538788.1:p.Met371= | |
XR_001736906.2:n.1749G= | ||
NM_005857.5:c.1362G= MANE Select | NP_005848.2:p.Met454= |