HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1433354C= , CM000667.2:g.1433354C= | GRCh38 |
NC_000005.9:g.1433469C= , CM000667.1:g.1433469C= | GRCh37 |
NC_000005.8:g.1486469C= | NCBI36 |
NG_015885.1:g.17075G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.419-656G= MANE Select | ENSP00000270349.9:n.419-656G= | |
ENST00000270349.11:c.419-656G= | ENSP00000270349.9:n.419-656G= | |
NM_001044.4:c.419-656G= | NP_001035.1:n.419-656G= | |
NM_001044.5:c.419-656G= MANE Select | NP_001035.1:n.419-656G= |