HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48304026C= , CM000675.2:g.48304026C= | GRCh38 |
NC_000013.10:g.48878162C= , CM000675.1:g.48878162C= | GRCh37 |
NC_000013.9:g.47776163C= | NCBI36 |
NG_009009.1:g.5280C= , LRG_517:g.5280C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.114C= MANE Select | ENSP00000267163.4:p.Gly38= | |
ENST00000646097.1:c.114C= | ENSP00000496556.1:p.Gly38= | |
ENST00000650461.1:c.114C= | ENSP00000497193.1:p.Gly38= | |
ENST00000267163.4:c.114C= | ENSP00000267163.4:p.Gly38= | |
ENST00000467505.5:c.114C= | ENSP00000434702.1:p.Gly38= | |
ENST00000525036.1:n.276C= | ||
NM_000321.2:c.114C= , LRG_517t1:c.114C= | NP_000312.2:p.Gly38= | |
NM_000321.3:c.114C= MANE Select | NP_000312.2:p.Gly38= |