HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2274798C>G , CM000681.2:g.2274798C>G | GRCh38 |
NC_000019.9:g.2274797C>G , CM000681.1:g.2274797C>G | GRCh37 |
NC_000019.8:g.2225797C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342063.5:c.*882G>C MANE Select | ENSP00000345102.3:n.*882G>C | |
ENST00000342063.4:c.*882G>C | ENSP00000345102.3:n.*882G>C | |
ENST00000621615.1:c.146+5054C>G | ENSP00000481965.1:n.146+5054C>G | |
NM_198532.2:c.*882G>C | NP_940934.1:n.*882G>C | |
NM_198532.3:c.*882G>C MANE Select | NP_940934.1:n.*882G>C |