HGVS | Genome Assembly |
---|---|
NC_000005.10:g.52835481T>C , CM000667.2:g.52835481T>C | GRCh38 |
NC_000005.9:g.52131315T>C , CM000667.1:g.52131315T>C | GRCh37 |
NC_000005.8:g.52167072T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282588.7:c.62-13884T>C MANE Select | ENSP00000282588.5:n.62-13884T>C | |
ENST00000650673.1:c.62-13884T>C | ENSP00000498529.1:n.62-13884T>C | |
ENST00000282588.6:c.62-13884T>C | ENSP00000282588.5:n.62-13884T>C | |
NM_181501.1:c.62-13884T>C | NP_852478.1:n.62-13884T>C | |
NM_181501.2:c.62-13884T>C MANE Select | NP_852478.1:n.62-13884T>C |