HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022734G= , CM000663.2:g.17022734G= | GRCh38 |
NC_000001.10:g.17349229G= , CM000663.1:g.17349229G= | GRCh37 |
NC_000001.9:g.17221816G= | NCBI36 |
NG_012340.1:g.36437C= , LRG_316:g.36437C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.472-4C= | ENSP00000481376.2:n.472-4C= | |
ENST00000491274.6:c.601-4C= | ENSP00000480482.2:n.601-4C= | |
ENST00000375499.8:c.643-4C= MANE Select | ENSP00000364649.3:n.643-4C= | |
ENST00000375499.7:c.643-4C= | ENSP00000364649.3:n.643-4C= | |
ENST00000475049.5:n.68-4C= | ||
ENST00000485092.5:n.303C= | ||
ENST00000485515.5:n.577-4C= | ||
NM_003000.2:c.643-4C= , LRG_316t1:c.643-4C= | NP_002991.2:n.643-4C= | |
NM_003000.3:c.643-4C= MANE Select | NP_002991.2:n.643-4C= |