HGVS | Genome Assembly |
---|---|
NC_000010.11:g.86876011A= , CM000672.2:g.86876011A= | GRCh38 |
NC_000010.10:g.88635768A= , CM000672.1:g.88635768A= | GRCh37 |
NC_000010.9:g.88625748A= | NCBI36 |
NG_009362.1:g.124373A= , LRG_298:g.124373A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000480152.3:c.-8A= | ENSP00000483569.2:n.-8A= | |
ENST00000635816.2:c.-8A= | ENSP00000489707.1:n.-8A= | |
ENST00000636056.2:c.-8A= | ENSP00000490273.1:n.-8A= | |
ENST00000372037.8:c.-8A= MANE Select | ENSP00000361107.2:n.-8A= | |
ENST00000635816.1:c.-8A= | ENSP00000489707.1:n.-8A= | |
ENST00000636056.1:c.-8A= | ENSP00000490273.1:n.-8A= | |
ENST00000638429.1:c.-8A= | ENSP00000492290.1:n.-8A= | |
ENST00000372037.7:c.-8A= | ENSP00000361107.1:n.-8A= | |
ENST00000480152.2:c.-8A= | ENSP00000483569.1:n.-8A= | |
NM_004329.2:c.-8A= , LRG_298t1:c.-8A= | NP_004320.2:n.-8A= | |
XM_011540103.1:c.-8A= | XP_011538405.1:n.-8A= | |
XM_011540104.1:c.-8A= | XP_011538406.1:n.-8A= | |
XM_011540103.2:c.-8A= | XP_011538405.1:n.-8A= | |
XM_011540104.2:c.-8A= | XP_011538406.1:n.-8A= | |
NM_004329.3:c.-8A= MANE Select | NP_004320.2:n.-8A= |