HGVS | Genome Assembly |
---|---|
NC_000007.14:g.44541320G>A , CM000669.2:g.44541320G>A | GRCh38 |
NC_000007.13:g.44580919G>A , CM000669.1:g.44580919G>A | GRCh37 |
NC_000007.12:g.44547444G>A | NCBI36 |
NG_013088.1:g.4996C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381160.8:c.-61C>T MANE Select | ENSP00000370552.3:n.-61C>T | |
XM_011515327.1:c.-61C>T | XP_011513629.1:n.-61C>T | |
XM_011515326.3:c.-61C>T | XP_011513628.1:n.-61C>T | |
XR_002956423.1:n.332C>T | ||
NM_001101648.2:c.-61C>T MANE Select | NP_001095118.1:n.-61C>T | |
NM_001300967.2:c.-61C>T | NP_001287896.1:n.-61C>T | |
NM_013389.3:c.-61C>T | NP_037521.2:n.-61C>T |