HGVS | Genome Assembly |
---|---|
NC_000003.12:g.129061756C= , CM000665.2:g.129061756C= | GRCh38 |
NC_000003.11:g.128780599C= , CM000665.1:g.128780599C= | GRCh37 |
NC_000003.10:g.130263289C= | NCBI36 |
NG_008715.1:g.5955C= , LRG_477:g.5955C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307395.5:c.17C= MANE Select | ENSP00000303942.4:p.Ala6= | |
ENST00000307395.4:c.17C= | ENSP00000303942.4:p.Ala6= | |
NM_000174.4:c.17C= , LRG_477t1:c.17C= | NP_000165.1:p.Ala6= | |
XM_005247374.3:c.17C= | XP_005247431.1:p.Ala6= | |
XM_011512701.1:c.17C= | XP_011511003.1:p.Ala6= | |
XM_011512702.1:c.17C= | XP_011511004.1:p.Ala6= | |
NM_000174.5:c.17C= MANE Select | NP_000165.1:p.Ala6= |