HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155812390A= , CM000669.2:g.155812390A= | GRCh38 |
NC_000007.13:g.155605084A= , CM000669.1:g.155605084A= | GRCh37 |
NC_000007.12:g.155297845A= | NCBI36 |
NG_007504.2:g.4884T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297261.7:c.-268T= MANE Select | ENSP00000297261.2:n.-268T= | |
NM_000193.4:c.-268T= MANE Select | NP_000184.1:n.-268T= |