HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028852T= , CM000667.2:g.135028852T= | GRCh38 |
NC_000005.9:g.134364542T= , CM000667.1:g.134364542T= | GRCh37 |
NC_000005.8:g.134392441T= | NCBI36 |
NG_012114.1:g.10423A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.872A= MANE Select | ENSP00000265340.6:p.Gln291= | |
ENST00000265340.11:c.872A= | ENSP00000265340.6:p.Gln291= | |
ENST00000506438.5:c.872A= | ENSP00000427542.1:p.Gln291= | |
NM_002653.4:c.872A= | NP_002644.4:p.Gln291= | |
NM_002653.5:c.872A= MANE Select | NP_002644.4:p.Gln291= |