HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659442G>C , CM000685.2:g.136659442G>C | GRCh38 |
NC_000023.10:g.135741601G>C , CM000685.1:g.135741601G>C | GRCh37 |
NC_000023.9:g.135569267G>C | NCBI36 |
NG_007280.1:g.16266G>C , LRG_141:g.16266G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*431G>C | ENSP00000512122.1:n.*431G>C | |
ENST00000695725.1:c.*368G>C | ENSP00000512123.1:n.*368G>C | |
ENST00000695726.1:n.2781G>C | ||
ENST00000695729.1:n.3616G>C | ||
ENST00000370629.7:c.*27G>C MANE Select | ENSP00000359663.2:n.*27G>C | |
ENST00000370628.2:c.*27G>C | ENSP00000359662.2:n.*27G>C | |
ENST00000370629.6:c.*27G>C | ENSP00000359663.2:n.*27G>C | |
NM_000074.2:c.*27G>C , LRG_141t1:c.*27G>C | NP_000065.1:n.*27G>C | |
NM_000074.3:c.*27G>C MANE Select | NP_000065.1:n.*27G>C |