HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1423682T= , CM000667.2:g.1423682T= | GRCh38 |
NC_000005.9:g.1423797T= , CM000667.1:g.1423797T= | GRCh37 |
NC_000005.8:g.1476797T= | NCBI36 |
NG_015885.1:g.26747A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.654-1668A= MANE Select | ENSP00000270349.9:n.654-1668A= | |
ENST00000270349.11:c.654-1668A= | ENSP00000270349.9:n.654-1668A= | |
NM_001044.4:c.654-1668A= | NP_001035.1:n.654-1668A= | |
NM_001044.5:c.654-1668A= MANE Select | NP_001035.1:n.654-1668A= |