HGVS | Genome Assembly |
---|---|
NC_000010.11:g.102837314A>G , CM000672.2:g.102837314A>G | GRCh38 |
NC_000010.10:g.104597071A>G , CM000672.1:g.104597071A>G | GRCh37 |
NC_000010.9:g.104587061A>G | NCBI36 |
NG_007955.1:g.5220T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369887.4:c.48T>C MANE Select | ENSP00000358903.3:p.Phe16= | |
ENST00000638190.1:c.48T>C | ENSP00000492539.1:p.Phe16= | |
ENST00000638272.1:c.48T>C | ENSP00000491508.1:p.Phe16= | |
ENST00000638971.1:c.48T>C | ENSP00000492313.1:p.Phe16= | |
ENST00000639393.1:c.48T>C | ENSP00000492651.1:p.Phe16= | |
ENST00000369887.3:c.48T>C | ENSP00000358903.3:p.Phe16= | |
ENST00000489268.1:n.101T>C | ||
NM_000102.3:c.48T>C | NP_000093.1:p.Phe16= | |
NM_000102.4:c.48T>C MANE Select | NP_000093.1:p.Phe16= |