HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157241417T>C , CM000667.2:g.157241417T>C | GRCh38 |
NC_000005.9:g.156668427T>C , CM000667.1:g.156668427T>C | GRCh37 |
NC_000005.8:g.156601005T>C | NCBI36 |
NG_016276.1:g.65521T>C , LRG_189:g.65521T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696962.1:c.852-229T>C | ENSP00000513001.1:n.852-229T>C | |
ENST00000422843.8:c.986-229T>C MANE Select | ENSP00000398655.4:n.986-229T>C | |
ENST00000422843.7:c.986-229T>C | ENSP00000398655.3:n.986-229T>C | |
ENST00000519402.5:n.2342T>C | ||
ENST00000520173.1:n.104-229T>C | ||
NM_005546.3:c.986-229T>C , LRG_189t1:c.986-229T>C | NP_005537.3:n.986-229T>C | |
XM_017009443.1:c.611-229T>C | XP_016864932.1:n.611-229T>C | |
NM_005546.4:c.986-229T>C MANE Select | NP_005537.3:n.986-229T>C |