HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111072454T= , CM000667.2:g.111072454T= | GRCh38 |
NC_000005.9:g.110408152T= , CM000667.1:g.110408152T= | GRCh37 |
NC_000005.8:g.110436051T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.171+393T= MANE Select | ENSP00000339804.3:n.171+393T= | |
ENST00000344895.3:c.171+393T= | ENSP00000339804.3:n.171+393T= | |
ENST00000420978.6:c.171+393T= | ENSP00000399099.2:n.171+393T= | |
NM_033035.4:c.171+393T= | NP_149024.1:n.171+393T= | |
NR_045089.1:n.1575+393T= | ||
NM_033035.5:c.171+393T= MANE Select | NP_149024.1:n.171+393T= | |
NR_045089.2:n.1593+393T= |