HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584722T= , CM000673.2:g.67584722T= | GRCh38 |
NC_000011.9:g.67352193T= , CM000673.1:g.67352193T= | GRCh37 |
NC_000011.8:g.67108769T= | NCBI36 |
NG_012075.1:g.6128T= , LRG_723:g.6128T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.182T= | ENSP00000381604.1:p.Leu61= | |
ENST00000398606.10:c.182T= MANE Select | ENSP00000381607.3:p.Leu61= | |
ENST00000646888.1:c.75T= | ENSP00000494477.1:p.Pro25= | |
ENST00000398603.5:c.182T= | ENSP00000381604.1:p.Leu61= | |
ENST00000398606.7:c.182T= | ENSP00000381607.3:p.Leu61= | |
ENST00000489040.1:n.181T= | ||
ENST00000494593.1:n.612T= | ||
ENST00000498765.5:c.145T= | ||
NM_000852.3:c.182T= , LRG_723t1:c.182T= | NP_000843.1:p.Leu61= | |
NM_000852.4:c.182T= MANE Select | NP_000843.1:p.Leu61= |