HGVS | Genome Assembly |
---|---|
NC_000006.12:g.30163346T>G , CM000668.2:g.30163346T>G | GRCh38 |
NC_000006.11:g.30131123T>G , CM000668.1:g.30131123T>G | GRCh37 |
NC_000006.10:g.30239102T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376694.8:c.-339T>G (TRIM15) | ENSP00000365884.4:n.-339T>G | |
ENST00000619857.4:c.-546T>G (TRIM15) | ENSP00000484001.1:n.-546T>G | |
NM_033229.2:c.-339T>G (TRIM15) | NP_150232.2:n.-339T>G | |
XM_011514224.1:c.-423+61A>C (TRIM10) | XP_011512526.1:n.-423+61A>C |