HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312925G>T , CM000673.2:g.118312925G>T | GRCh38 |
NC_000011.9:g.118183640G>T , CM000673.1:g.118183640G>T | GRCh37 |
NC_000011.8:g.117688850G>T | NCBI36 |
NG_007383.1:g.13346G>T , LRG_38:g.13346G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.352+59G>T MANE Select | ENSP00000354566.4:n.352+59G>T | |
ENST00000361763.8:c.352+59G>T | ENSP00000354566.4:n.352+59G>T | |
ENST00000526146.5:n.957G>T | ||
ENST00000528435.5:n.905+59G>T | ||
ENST00000528600.1:c.334+59G>T | ENSP00000433975.1:n.334+59G>T | |
ENST00000529713.5:n.517G>T | ||
ENST00000531913.1:n.723+59G>T | ||
NM_000733.3:c.352+59G>T , LRG_38t1:c.352+59G>T | NP_000724.1:n.352+59G>T | |
NM_000733.4:c.352+59G>T MANE Select | NP_000724.1:n.352+59G>T |