HGVS | Genome Assembly |
---|---|
NC_000007.14:g.129210508A>C , CM000669.2:g.129210508A>C | GRCh38 |
NC_000007.13:g.128850349A>C , CM000669.1:g.128850349A>C | GRCh37 |
NC_000007.12:g.128637585A>C | NCBI36 |
NG_023340.1:g.26637A>C | |
NG_023340.2:g.26637A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000249373.8:c.1612A>C MANE Select | ENSP00000249373.3:p.Thr538Pro | |
ENST00000655644.1:c.*1367A>C | ENSP00000499377.1:n.*1367A>C | |
ENST00000249373.7:c.1612A>C | ENSP00000249373.3:p.Thr538Pro | |
ENST00000462420.2:c.583A>C | ||
ENST00000475779.1:c.1A>C | ENSP00000420749.1:p.Thr1Pro | |
NM_005631.4:c.1612A>C | NP_005622.1:p.Thr538Pro | |
XM_011516522.1:c.1222A>C | XP_011514824.1:p.Thr408Pro | |
XM_024446891.1:c.1222A>C | XP_024302659.1:p.Thr408Pro | |
NM_005631.5:c.1612A>C MANE Select | NP_005622.1:p.Thr538Pro |