HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117837178T>C , CM000670.2:g.117837178T>C | GRCh38 |
NC_000008.10:g.118849417T>C , CM000670.1:g.118849417T>C | GRCh37 |
NC_000008.9:g.118918598T>C | NCBI36 |
NG_007455.2:g.279642A>G , LRG_493:g.279642A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.453A>G | ||
ENST00000378204.7:c.986A>G MANE Select | ENSP00000367446.3:p.His329Arg | |
ENST00000436216.2:c.354A>G | ||
ENST00000378204.6:c.986A>G | ENSP00000367446.2:p.His329Arg | |
ENST00000436216.1:c.354A>G | ||
ENST00000437196.1:c.74-1627A>G | ENSP00000407299.1:n.74-1627A>G | |
NM_000127.2:c.986A>G , LRG_493t1:c.986A>G | NP_000118.2:p.His329Arg | |
NM_000127.3:c.986A>G MANE Select | NP_000118.2:p.His329Arg |