HGVS | Genome Assembly |
---|---|
NC_000004.12:g.154583796_154583797insA , CM000666.2:g.154583796_154583797insA | GRCh38 |
NC_000004.11:g.155504948_155504949insA , CM000666.1:g.155504948_155504949insA | GRCh37 |
NC_000004.10:g.155724398_155724399insA | NCBI36 |
NG_008832.1:g.11949_11950insT , LRG_557:g.11949_11950insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651975.2:c.*327_*328insT | ENSP00000498441.1:n.*327_*328insT | |
ENST00000651975.1:c.*327_*328insT | ENSP00000498441.1:n.*327_*328insT | |
ENST00000302053.7:c.*327_*328insT | ENSP00000306361.3:n.*327_*328insT | |
NM_000508.3:c.*327_*328insT , LRG_557t1:c.*327_*328insT | NP_000499.1:n.*327_*328insT | |
NM_000508.4:c.*327_*328insT | NP_000499.1:n.*327_*328insT | |
NM_000508.5:c.*327_*328insT | NP_000499.1:n.*327_*328insT |