HGVS | Genome Assembly |
---|---|
NC_000014.9:g.52322369C>G , CM000676.2:g.52322369C>G | GRCh38 |
NC_000014.8:g.52789087C>G , CM000676.1:g.52789087C>G | GRCh37 |
NC_000014.7:g.51858837C>G | NCBI36 |
NG_013082.1:g.13072C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000245457.6:c.844-4852C>G MANE Select | ENSP00000245457.5:n.844-4852C>G | |
ENST00000245457.5:c.844-4852C>G | ENSP00000245457.5:n.844-4852C>G | |
ENST00000557436.1:c.79-4852C>G | ENSP00000450933.1:n.79-4852C>G | |
NM_000956.3:c.844-4852C>G | NP_000947.2:n.844-4852C>G | |
NM_000956.4:c.844-4852C>G MANE Select | NP_000947.2:n.844-4852C>G |