HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312619A= , CM000673.2:g.118312619A= | GRCh38 |
NC_000011.9:g.118183334A= , CM000673.1:g.118183334A= | GRCh37 |
NC_000011.8:g.117688544A= | NCBI36 |
NG_007383.1:g.13040A= , LRG_38:g.13040A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361763.9:c.105A= MANE Select | ENSP00000354566.4:p.Pro35= | |
ENST00000361763.8:c.105A= | ENSP00000354566.4:p.Pro35= | |
ENST00000526146.5:n.651A= | ||
ENST00000528435.5:n.658A= | ||
ENST00000528600.1:c.87A= | ENSP00000433975.1:p.Ala29= | |
ENST00000529713.5:n.211A= | ||
ENST00000531913.1:n.476A= | ||
NM_000733.3:c.105A= , LRG_38t1:c.105A= | NP_000724.1:p.Pro35= | |
NM_000733.4:c.105A= MANE Select | NP_000724.1:p.Pro35= |