HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117835502G>T , CM000670.2:g.117835502G>T | GRCh38 |
NC_000008.10:g.118847741G>T , CM000670.1:g.118847741G>T | GRCh37 |
NC_000008.9:g.118916922G>T | NCBI36 |
NG_007455.2:g.281318C>A , LRG_493:g.281318C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.573C>A | ||
ENST00000378204.7:c.1106C>A MANE Select | ENSP00000367446.3:p.Ser369Tyr | |
ENST00000436216.2:c.474C>A | ||
ENST00000378204.6:c.1106C>A | ENSP00000367446.2:p.Ser369Tyr | |
ENST00000436216.1:c.474C>A | ||
ENST00000437196.1:c.123C>A | ENSP00000407299.1:p.Leu41= | |
NM_000127.2:c.1106C>A , LRG_493t1:c.1106C>A | NP_000118.2:p.Ser369Tyr | |
NM_000127.3:c.1106C>A MANE Select | NP_000118.2:p.Ser369Tyr |