HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117835517C>G , CM000670.2:g.117835517C>G | GRCh38 |
NC_000008.10:g.118847756C>G , CM000670.1:g.118847756C>G | GRCh37 |
NC_000008.9:g.118916937C>G | NCBI36 |
NG_007455.2:g.281303G>C , LRG_493:g.281303G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.558G>C | ||
ENST00000378204.7:c.1091G>C MANE Select | ENSP00000367446.3:p.Trp364Ser | |
ENST00000436216.2:c.459G>C | ||
ENST00000378204.6:c.1091G>C | ENSP00000367446.2:p.Trp364Ser | |
ENST00000436216.1:c.459G>C | ||
ENST00000437196.1:c.108G>C | ENSP00000407299.1:p.Met36Ile | |
NM_000127.2:c.1091G>C , LRG_493t1:c.1091G>C | NP_000118.2:p.Trp364Ser | |
NM_000127.3:c.1091G>C MANE Select | NP_000118.2:p.Trp364Ser |