HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219060458C= , CM000664.2:g.219060458C= | GRCh38 |
NC_000002.11:g.219925180C= , CM000664.1:g.219925180C= | GRCh37 |
NC_000002.10:g.219633424C= | NCBI36 |
NG_016741.1:g.5059G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295731.7:c.10G= MANE Select | ENSP00000295731.5:p.Ala4= | |
ENST00000295731.6:c.10G= | ENSP00000295731.5:p.Ala4= | |
NM_002181.3:c.10G= | NP_002172.2:p.Ala4= | |
NM_002181.4:c.10G= MANE Select | NP_002172.2:p.Ala4= |