HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128248757C>T , CM000669.2:g.128248757C>T | GRCh38 |
NC_000007.13:g.127888810C>T , CM000669.1:g.127888810C>T | GRCh37 |
NC_000007.12:g.127676046C>T | NCBI36 |
NG_007450.1:g.12480C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308868.5:c.-28-3234C>T MANE Select | ENSP00000312652.4:n.-28-3234C>T | |
ENST00000308868.4:c.-28-3234C>T | ENSP00000312652.4:n.-28-3234C>T | |
NM_000230.2:c.-28-3234C>T | NP_000221.1:n.-28-3234C>T | |
XM_005250340.3:c.-28-3234C>T | XP_005250397.1:n.-28-3234C>T | |
XM_005250340.5:c.-28-3234C>T | XP_005250397.1:n.-28-3234C>T | |
NM_000230.3:c.-28-3234C>T MANE Select | NP_000221.1:n.-28-3234C>T |