HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25004843G>A , CM000685.2:g.25004843G>A | GRCh38 |
NC_000023.10:g.25022960G>A , CM000685.1:g.25022960G>A | GRCh37 |
NC_000023.9:g.24932881G>A | NCBI36 |
NG_008281.1:g.16106C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.1516C>T MANE Select | ENSP00000368332.4:p.Pro506Ser | |
ENST00000379044.4:c.1516C>T | ENSP00000368332.4:p.Pro506Ser | |
NM_139058.2:c.1516C>T | NP_620689.1:p.Pro506Ser | |
NM_139058.3:c.1516C>T MANE Select | NP_620689.1:p.Pro506Ser |