HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110914195T>G , CM000674.2:g.110914195T>G | GRCh38 |
NC_000012.11:g.111351999T>G , CM000674.1:g.111351999T>G | GRCh37 |
NC_000012.10:g.109836382T>G | NCBI36 |
NG_007554.1:g.11383A>C , LRG_393:g.11383A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000228841.15:c.265A>C MANE Select | ENSP00000228841.8:p.Lys89Gln | |
ENST00000663220.1:c.208A>C | ENSP00000499568.1:p.Lys70Gln | |
ENST00000228841.12:c.265A>C | ENSP00000228841.7:p.Lys89Gln | |
ENST00000548438.1:c.223A>C | ENSP00000447154.1:p.Lys75Gln | |
ENST00000549029.1:n.96A>C | ||
NM_000432.3:c.265A>C , LRG_393t1:c.265A>C | NP_000423.2:p.Lys89Gln | |
NM_000432.4:c.265A>C MANE Select | NP_000423.2:p.Lys89Gln |