HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104064579C= , CM000672.2:g.104064579C= | GRCh38 |
NC_000010.10:g.105824337C= , CM000672.1:g.105824337C= | GRCh37 |
NC_000010.9:g.105814327C= | NCBI36 |
NG_007069.1:g.26302G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.625G= | ENSP00000358748.3:p.Ala209= | |
ENST00000648076.2:c.625G= MANE Select | ENSP00000497653.1:p.Ala209= | |
ENST00000649118.1:n.740G= | ||
ENST00000650263.1:c.577G= | ENSP00000497850.1:p.Ala193= | |
ENST00000353479.9:c.625G= | ENSP00000340937.5:p.Ala209= | |
ENST00000369733.7:c.625G= | ENSP00000358748.3:p.Ala209= | |
ENST00000393211.3:c.625G= | ENSP00000376905.3:p.Ala209= | |
NM_000494.3:c.625G= | NP_000485.3:p.Ala209= | |
NM_000494.4:c.625G= MANE Select | NP_000485.3:p.Ala209= |