HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1433379A>G , CM000667.2:g.1433379A>G | GRCh38 |
NC_000005.9:g.1433494A>G , CM000667.1:g.1433494A>G | GRCh37 |
NC_000005.8:g.1486494A>G | NCBI36 |
NG_015885.1:g.17050T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.419-681T>C MANE Select | ENSP00000270349.9:n.419-681T>C | |
ENST00000270349.11:c.419-681T>C | ENSP00000270349.9:n.419-681T>C | |
NM_001044.4:c.419-681T>C | NP_001035.1:n.419-681T>C | |
NM_001044.5:c.419-681T>C MANE Select | NP_001035.1:n.419-681T>C |