HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21816626C>A , CM000669.2:g.21816626C>A | GRCh38 |
NC_000007.13:g.21856244C>A , CM000669.1:g.21856244C>A | GRCh37 |
NC_000007.12:g.21822769C>A | NCBI36 |
NG_012886.2:g.278412C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.10492C>A MANE Select | ENSP00000475939.1:p.Pro3498Thr | |
ENST00000328843.10:c.10513C>A | ENSP00000330671.7:p.Pro3505Thr | |
ENST00000409508.7:c.10492C>A | ENSP00000475939.1:p.Pro3498Thr | |
ENST00000620169.4:c.10513C>A | ENSP00000481693.1:p.Pro3505Thr | |
NM_001277115.1:c.10492C>A | NP_001264044.1:p.Pro3498Thr | |
NM_001277115.2:c.10492C>A MANE Select | NP_001264044.1:p.Pro3498Thr |