HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157241287T= , CM000667.2:g.157241287T= | GRCh38 |
NC_000005.9:g.156668297T= , CM000667.1:g.156668297T= | GRCh37 |
NC_000005.8:g.156600875T= | NCBI36 |
NG_016276.1:g.65391T= , LRG_189:g.65391T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696962.1:c.852-359T= | ENSP00000513001.1:n.852-359T= | |
ENST00000422843.8:c.986-359T= MANE Select | ENSP00000398655.4:n.986-359T= | |
ENST00000422843.7:c.986-359T= | ENSP00000398655.3:n.986-359T= | |
ENST00000519402.5:n.2212T= | ||
ENST00000520173.1:n.104-359T= | ||
NM_005546.3:c.986-359T= , LRG_189t1:c.986-359T= | NP_005537.3:n.986-359T= | |
XM_017009443.1:c.611-359T= | XP_016864932.1:n.611-359T= | |
NM_005546.4:c.986-359T= MANE Select | NP_005537.3:n.986-359T= |