HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584757C= , CM000673.2:g.67584757C= | GRCh38 |
NC_000011.9:g.67352228C= , CM000673.1:g.67352228C= | GRCh37 |
NC_000011.8:g.67108804C= | NCBI36 |
NG_012075.1:g.6163C= , LRG_723:g.6163C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.217C= | ENSP00000381604.1:p.Leu73= | |
ENST00000398606.10:c.217C= MANE Select | ENSP00000381607.3:p.Leu73= | |
ENST00000646888.1:c.110C= | ENSP00000494477.1:p.Pro37= | |
ENST00000398603.5:c.217C= | ENSP00000381604.1:p.Leu73= | |
ENST00000398606.7:c.217C= | ENSP00000381607.3:p.Leu73= | |
ENST00000489040.1:n.216C= | ||
ENST00000494593.1:n.647C= | ||
ENST00000498765.5:c.180C= | ||
NM_000852.3:c.217C= , LRG_723t1:c.217C= | NP_000843.1:p.Leu73= | |
NM_000852.4:c.217C= MANE Select | NP_000843.1:p.Leu73= |