HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35849093G>C , CM000681.2:g.35849093G>C | GRCh38 |
NC_000019.9:g.36339995G>C , CM000681.1:g.36339995G>C | GRCh37 |
NC_000019.8:g.41031835G>C | NCBI36 |
NG_013356.2:g.25195C>G , LRG_693:g.25195C>G | |
NG_051206.1:g.2459G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.895C>G MANE Select | ENSP00000368190.4:p.Arg299Gly | |
ENST00000353632.6:c.895C>G | ENSP00000343634.5:p.Arg299Gly | |
ENST00000378910.9:c.895C>G | ENSP00000368190.4:p.Arg299Gly | |
NM_004646.3:c.895C>G , LRG_693t1:c.895C>G | NP_004637.1:p.Arg299Gly | |
NM_004646.4:c.895C>G MANE Select | NP_004637.1:p.Arg299Gly |