HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013556C>G , CM000685.2:g.25013556C>G | GRCh38 |
NC_000023.10:g.25031673C>G , CM000685.1:g.25031673C>G | GRCh37 |
NC_000023.9:g.24941594C>G | NCBI36 |
NG_008281.1:g.7393G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.439G>C MANE Select | ENSP00000368332.4:p.Ala147Pro | |
ENST00000379044.4:c.439G>C | ENSP00000368332.4:p.Ala147Pro | |
NM_139058.2:c.439G>C | NP_620689.1:p.Ala147Pro | |
NM_139058.3:c.439G>C MANE Select | NP_620689.1:p.Ala147Pro |