HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215766712A>G , CM000663.2:g.215766712A>G | GRCh38 |
NC_000001.10:g.215940054A>G , CM000663.1:g.215940054A>G | GRCh37 |
NC_000001.9:g.214006677A>G | NCBI36 |
NG_009497.1:g.661685T>C | |
NG_009497.2:g.661737T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.11016T>C MANE Select | ENSP00000305941.3:p.Phe3672= | |
ENST00000674083.1:c.11016T>C | ENSP00000501296.1:p.Phe3672= | |
ENST00000307340.7:c.11016T>C | ENSP00000305941.3:p.Phe3672= | |
NM_206933.2:c.11016T>C | NP_996816.2:p.Phe3672= | |
NM_206933.3:c.11016T>C | NP_996816.2:p.Phe3672= | |
NM_206933.4:c.11016T>C MANE Select | NP_996816.3:p.Phe3672= |