HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116822667C= , CM000673.2:g.116822667C= | GRCh38 |
NC_000011.9:g.116693383C= , CM000673.1:g.116693383C= | GRCh37 |
NC_000011.8:g.116198593C= | NCBI36 |
NG_012044.1:g.5629G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357780.5:c.168G= MANE Select | ENSP00000350425.3:p.Gln56= | |
ENST00000357780.4:c.168G= | ENSP00000350425.3:p.Gln56= | |
NM_000482.3:c.168G= | NP_000473.2:p.Gln56= | |
NM_000482.4:c.168G= MANE Select | NP_000473.2:p.Gln56= |