HGVS | Genome Assembly |
---|---|
NC_000006.12:g.135055071T= , CM000668.2:g.135055071T= | GRCh38 |
NC_000006.11:g.135376209T= , CM000668.1:g.135376209T= | GRCh37 |
NC_000006.10:g.135417902T= | NCBI36 |
NG_012002.1:g.4828A= |
HGVS | Amino-acid Change |
---|---|
ENST00000529882.5:c.89-4424A= | ENSP00000433030.1:n.89-4424A= |