HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136055777G>T , CM000667.2:g.136055777G>T | GRCh38 |
NC_000005.9:g.135391466G>T , CM000667.1:g.135391466G>T | GRCh37 |
NC_000005.8:g.135419365G>T | NCBI36 |
NG_012646.1:g.31883G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.1508G>T MANE Select | ENSP00000416330.2:p.Gly503Val | |
ENST00000442011.6:c.1508G>T | ENSP00000416330.2:p.Gly503Val | |
ENST00000506699.5:n.2025G>T | ||
ENST00000507018.5:c.1486G>T | ||
ENST00000509485.5:c.423G>T | ||
ENST00000514242.5:n.279G>T | ||
ENST00000514554.5:c.660G>T | ||
NM_000358.2:c.1508G>T | NP_000349.1:p.Gly503Val | |
NM_000358.3:c.1508G>T MANE Select | NP_000349.1:p.Gly503Val |