HGVS | Genome Assembly |
---|---|
NC_000017.11:g.73196269C>T , CM000679.2:g.73196269C>T | GRCh38 |
NC_000017.10:g.71192408C>T , CM000679.1:g.71192408C>T | GRCh37 |
NC_000017.9:g.68704003C>T | NCBI36 |
NG_008971.1:g.8236C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299886.9:c.316-238C>T MANE Select | ENSP00000299886.4:n.316-238C>T | |
ENST00000299886.8:c.316-238C>T | ENSP00000299886.4:n.316-238C>T | |
ENST00000438720.7:c.314-238C>T | ||
ENST00000582587.2:c.293-218C>T | ||
ENST00000618996.4:c.316-238C>T | ENSP00000479450.1:n.316-238C>T | |
NM_018714.2:c.316-238C>T | NP_061184.1:n.316-238C>T | |
NM_018714.3:c.316-238C>T MANE Select | NP_061184.1:n.316-238C>T |