HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117837149C>G , CM000670.2:g.117837149C>G | GRCh38 |
NC_000008.10:g.118849388C>G , CM000670.1:g.118849388C>G | GRCh37 |
NC_000008.9:g.118918569C>G | NCBI36 |
NG_007455.2:g.279671G>C , LRG_493:g.279671G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000684189.1:n.482G>C | ||
ENST00000378204.7:c.1015G>C MANE Select | ENSP00000367446.3:p.Gly339Arg | |
ENST00000436216.2:c.383G>C | ||
ENST00000378204.6:c.1015G>C | ENSP00000367446.2:p.Gly339Arg | |
ENST00000436216.1:c.383G>C | ||
ENST00000437196.1:c.74-1598G>C | ENSP00000407299.1:n.74-1598G>C | |
NM_000127.2:c.1015G>C , LRG_493t1:c.1015G>C | NP_000118.2:p.Gly339Arg | |
NM_000127.3:c.1015G>C MANE Select | NP_000118.2:p.Gly339Arg |