HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884733G>A , CM000680.2:g.13884733G>A | GRCh38 |
NC_000018.9:g.13884732G>A , CM000680.1:g.13884732G>A | GRCh37 |
NC_000018.8:g.13874732G>A | NCBI36 |
NG_011819.1:g.35804C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.786C>T MANE Select | ENSP00000333821.2:p.Gly262= | |
ENST00000327606.3:c.786C>T | ENSP00000333821.2:p.Gly262= | |
NM_000529.2:c.786C>T MANE Select | NP_000520.1:p.Gly262= | |
NM_001291911.1:c.786C>T | NP_001278840.1:p.Gly262= | |
XM_017025781.1:c.786C>T | XP_016881270.1:p.Gly262= |