HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680348C>T , CM000663.2:g.186680348C>T | GRCh38 |
NC_000001.10:g.186649480C>T , CM000663.1:g.186649480C>T | GRCh37 |
NC_000001.9:g.184916103C>T | NCBI36 |
NG_028206.2:g.5080G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.-58G>A MANE Select | ENSP00000356438.5:n.-58G>A | |
ENST00000680451.1:c.-58G>A | ENSP00000506242.1:n.-58G>A | |
ENST00000681605.1:c.-58G>A | ENSP00000504900.1:n.-58G>A | |
ENST00000367468.9:c.-58G>A | ENSP00000356438.5:n.-58G>A | |
ENST00000490885.6:n.76G>A | ||
ENST00000559800.1:n.76G>A | ||
NM_000963.3:c.-58G>A | NP_000954.1:n.-58G>A | |
NM_000963.4:c.-58G>A MANE Select | NP_000954.1:n.-58G>A |