HGVS | Genome Assembly |
---|---|
NC_000016.10:g.30993200G>T , CM000678.2:g.30993200G>T | GRCh38 |
NC_000016.9:g.31004521G>T , CM000678.1:g.31004521G>T | GRCh37 |
NC_000016.8:g.30912022G>T | NCBI36 |
NG_041829.1:g.22309C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215095.11:c.716C>A MANE Select | ENSP00000215095.5:p.Ser239Tyr | |
ENST00000565419.2:c.716C>A | ENSP00000455899.1:p.Ser239Tyr | |
ENST00000215095.9:c.716C>A | ENSP00000215095.5:p.Ser239Tyr | |
ENST00000565419.1:c.716C>A | ENSP00000455899.1:p.Ser239Tyr | |
ENST00000569638.5:c.464C>A | ENSP00000457067.1:p.Ser155Tyr | |
NM_052874.4:c.716C>A | NP_443106.1:p.Ser239Tyr | |
XM_017022893.1:c.698C>A | XP_016878382.1:p.Ser233Tyr | |
NM_052874.5:c.716C>A MANE Select | NP_443106.1:p.Ser239Tyr |