HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47283170G>C , CM000679.2:g.47283170G>C | GRCh38 |
NC_000017.10:g.45360536G>C , CM000679.1:g.45360536G>C | GRCh37 |
NC_000017.9:g.42715535G>C | NCBI36 |
NG_008332.2:g.34329G>C , LRG_481:g.34329G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.166-184G>C | ENSP00000513002.1:n.166-184G>C | |
ENST00000559488.7:c.166-184G>C MANE Select | ENSP00000452786.2:n.166-184G>C | |
ENST00000559488.5:c.166-184G>C | ENSP00000452786.1:n.166-184G>C | |
ENST00000560629.1:c.131-184G>C | ||
ENST00000571680.1:c.166-184G>C | ENSP00000461626.1:n.166-184G>C | |
NM_000212.2:c.166-184G>C , LRG_481t1:c.166-184G>C | NP_000203.2:n.166-184G>C | |
NM_000212.3:c.166-184G>C MANE Select | NP_000203.2:n.166-184G>C |