HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101686824G>C , CM000671.2:g.101686824G>C | GRCh38 |
NC_000009.11:g.104449106G>C , CM000671.1:g.104449106G>C | GRCh37 |
NC_000009.10:g.103488927G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.1076C>G MANE Select | ENSP00000355155.3:p.Ser359Cys | |
ENST00000361820.3:c.1076C>G | ENSP00000355155.3:p.Ser359Cys | |
NM_133445.2:c.1076C>G | NP_597702.2:p.Ser359Cys | |
XM_011518211.1:c.1076C>G | XP_011516513.1:p.Ser359Cys | |
XM_011518212.1:c.1076C>G | XP_011516514.1:p.Ser359Cys | |
XR_929711.1:n.1163C>G | ||
XM_011518211.2:c.1076C>G | XP_011516513.1:p.Ser359Cys | |
NM_133445.3:c.1076C>G MANE Select | NP_597702.2:p.Ser359Cys |