HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1428040A= , CM000667.2:g.1428040A= | GRCh38 |
NC_000005.9:g.1428155A= , CM000667.1:g.1428155A= | GRCh37 |
NC_000005.8:g.1481155A= | NCBI36 |
NG_015885.1:g.22389T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.653+4424T= MANE Select | ENSP00000270349.9:n.653+4424T= | |
ENST00000270349.11:c.653+4424T= | ENSP00000270349.9:n.653+4424T= | |
NM_001044.4:c.653+4424T= | NP_001035.1:n.653+4424T= | |
NM_001044.5:c.653+4424T= MANE Select | NP_001035.1:n.653+4424T= |