HGVS | Genome Assembly |
---|---|
NC_000001.11:g.43349307A>G , CM000663.2:g.43349307A>G | GRCh38 |
NC_000001.10:g.43814978A>G , CM000663.1:g.43814978A>G | GRCh37 |
NC_000001.9:g.43587565A>G | NCBI36 |
NG_007525.1:g.16504A>G , LRG_510:g.16504A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372470.9:c.1513A>G MANE Select | ENSP00000361548.3:p.Ser505Gly | |
ENST00000413998.7:c.1492A>G | ENSP00000414004.3:p.Ser498Gly | |
ENST00000638732.1:n.1513A>G | ||
ENST00000643351.1:c.45A>G | ||
ENST00000372470.7:c.1513A>G | ENSP00000361548.3:p.Ser505Gly | |
ENST00000413998.6:c.1513A>G | ENSP00000414004.2:p.Ser505Gly | |
ENST00000612993.1:c.1513A>G | ENSP00000480273.1:p.Ser505Gly | |
NM_005373.2:c.1513A>G , LRG_510t1:c.1513A>G | NP_005364.1:p.Ser505Gly | |
XM_011541478.1:c.1492A>G | XP_011539780.1:p.Ser498Gly | |
XM_017001320.1:c.1684A>G | XP_016856809.1:p.Ser562Gly | |
NM_005373.3:c.1513A>G MANE Select | NP_005364.1:p.Ser505Gly |