HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21559224C= , CM000669.2:g.21559224C= | GRCh38 |
NC_000007.13:g.21598842C= , CM000669.1:g.21598842C= | GRCh37 |
NC_000007.12:g.21565367C= | NCBI36 |
NG_012886.2:g.21010C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.692+226C= MANE Select | ENSP00000475939.1:n.692+226C= | |
ENST00000328843.10:c.692+226C= | ENSP00000330671.7:n.692+226C= | |
ENST00000409508.7:c.692+226C= | ENSP00000475939.1:n.692+226C= | |
ENST00000620169.4:c.692+226C= | ENSP00000481693.1:n.692+226C= | |
NM_001277115.1:c.692+226C= | NP_001264044.1:n.692+226C= | |
NM_001277115.2:c.692+226C= MANE Select | NP_001264044.1:n.692+226C= |