HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780586A>C , CM000672.2:g.94780586A>C | GRCh38 |
NC_000010.10:g.96540343A>C , CM000672.1:g.96540343A>C | GRCh37 |
NC_000010.9:g.96530333A>C | NCBI36 |
NG_008384.2:g.22881A>C | |
NG_008384.3:g.22906A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.569A>C MANE Select | ENSP00000360372.3:p.Lys190Thr | |
ENST00000645461.1:n.1622A>C | ||
ENST00000371321.7:c.569A>C | ENSP00000360372.3:p.Lys190Thr | |
ENST00000464755.1:c.1332A>C | ENSP00000483243.1:n.1332A>C | |
NM_000769.2:c.569A>C | NP_000760.1:p.Lys190Thr | |
NM_000769.4:c.569A>C MANE Select | NP_000760.1:p.Lys190Thr |