HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218659A>C , CM000676.2:g.93218659A>C | GRCh38 |
NC_000014.8:g.93685005A>C , CM000676.1:g.93685005A>C | GRCh37 |
NC_000014.7:g.92754758A>C | NCBI36 |
NG_051089.1:g.16604A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000013070.11:c.734A>C MANE Select | ENSP00000013070.6:p.Lys245Thr | |
ENST00000013070.10:c.734A>C | ENSP00000013070.6:p.Lys245Thr | |
ENST00000416753.5:c.506A>C | ENSP00000391706.2:p.Lys169Thr | |
ENST00000553674.1:c.*435A>C | ENSP00000450470.1:n.*435A>C | |
ENST00000553857.5:c.378+3378A>C | ||
ENST00000556871.5:c.443A>C | ENSP00000451022.1:p.Lys148Thr | |
NM_175748.3:c.734A>C | NP_786924.2:p.Lys245Thr | |
NR_038150.1:n.836A>C | ||
NM_175748.4:c.734A>C MANE Select | NP_786924.2:p.Lys245Thr | |
NR_038150.2:n.636A>C |