HGVS | Genome Assembly |
---|---|
NC_000011.10:g.44275528G= , CM000673.2:g.44275528G= | GRCh38 |
NC_000011.9:g.44297078G= , CM000673.1:g.44297078G= | GRCh37 |
NC_000011.8:g.44253654G= | NCBI36 |
NG_015809.1:g.39639C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000652299.1:c.597C= MANE Select | ENSP00000498217.1:p.Pro199= | |
ENST00000329255.3:c.597C= | ENSP00000332744.3:p.Pro199= | |
NM_021926.3:c.597C= | NP_068745.2:p.Pro199= | |
XM_011520264.1:c.597C= | XP_011518566.1:p.Pro199= | |
XM_011520265.1:c.75C= | XP_011518567.1:p.Pro25= | |
XM_011520266.1:c.75C= | XP_011518568.1:p.Pro25= | |
NM_021926.4:c.597C= MANE Select | NP_068745.2:p.Pro199= |