HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86671022T>C , CM000670.2:g.86671022T>C | GRCh38 |
NC_000008.10:g.87683250T>C , CM000670.1:g.87683250T>C | GRCh37 |
NC_000008.9:g.87752366T>C | NCBI36 |
NG_016980.1:g.77654A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.415A>G MANE Select | ENSP00000316605.5:p.Met139Val | |
ENST00000680314.1:n.176A>G | ||
ENST00000681746.1:c.415A>G | ENSP00000505959.1:p.Met139Val | |
ENST00000320005.5:c.415A>G | ENSP00000316605.5:p.Met139Val | |
NM_019098.4:c.415A>G | NP_061971.3:p.Met139Val | |
XM_011517138.1:c.1A>G | XP_011515440.1:p.Met1Val | |
XM_011517138.2:c.1A>G | XP_011515440.1:p.Met1Val | |
NM_019098.5:c.415A>G MANE Select | NP_061971.3:p.Met139Val |