HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35848114C>G , CM000681.2:g.35848114C>G | GRCh38 |
NC_000019.9:g.36339016C>G , CM000681.1:g.36339016C>G | GRCh37 |
NC_000019.8:g.41030856C>G | NCBI36 |
NG_013356.2:g.26174G>C , LRG_693:g.26174G>C | |
NG_051206.1:g.1480C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1367G>C MANE Select | ENSP00000368190.4:p.Arg456Pro | |
ENST00000353632.6:c.1367G>C | ENSP00000343634.5:p.Arg456Pro | |
ENST00000378910.9:c.1367G>C | ENSP00000368190.4:p.Arg456Pro | |
ENST00000592132.1:n.374G>C | ||
NM_004646.3:c.1367G>C , LRG_693t1:c.1367G>C | NP_004637.1:p.Arg456Pro | |
NM_004646.4:c.1367G>C MANE Select | NP_004637.1:p.Arg456Pro |