HGVS | Genome Assembly |
---|---|
NC_000012.12:g.119186995G= , CM000674.2:g.119186995G= | GRCh38 |
NC_000012.11:g.119624800G= , CM000674.1:g.119624800G= | GRCh37 |
NC_000012.10:g.118109183G= | NCBI36 |
NG_007953.2:g.13206G= , LRG_249:g.13206G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000281938.7:c.368-30G= MANE Select | ENSP00000281938.3:n.368-30G= | |
ENST00000674542.1:c.368-6704G= | ENSP00000502352.1:n.368-6704G= | |
ENST00000674715.1:n.541-30G= | ||
ENST00000675900.1:n.21+4959G= | ||
ENST00000676071.1:n.101-30G= | ||
ENST00000676244.1:n.74-30G= | ||
ENST00000281938.6:c.368-30G= | ENSP00000281938.2:n.368-30G= | |
ENST00000541798.1:c.91-30G= | ||
ENST00000542496.1:n.196G= | ||
NM_014365.2:c.368-30G= , LRG_249t1:c.368-30G= | NP_055180.1:n.368-30G= | |
NM_014365.3:c.368-30G= MANE Select | NP_055180.1:n.368-30G= |