HGVS | Genome Assembly |
---|---|
NC_000016.10:g.30993211G= , CM000678.2:g.30993211G= | GRCh38 |
NC_000016.9:g.31004532G= , CM000678.1:g.31004532G= | GRCh37 |
NC_000016.8:g.30912033G= | NCBI36 |
NG_041829.1:g.22298C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215095.11:c.705C= MANE Select | ENSP00000215095.5:p.Asn235= | |
ENST00000565419.2:c.705C= | ENSP00000455899.1:p.Asn235= | |
ENST00000215095.9:c.705C= | ENSP00000215095.5:p.Asn235= | |
ENST00000565419.1:c.705C= | ENSP00000455899.1:p.Asn235= | |
ENST00000569638.5:c.453C= | ENSP00000457067.1:p.Asn151= | |
NM_052874.4:c.705C= | NP_443106.1:p.Asn235= | |
XM_017022893.1:c.687C= | XP_016878382.1:p.Asn229= | |
NM_052874.5:c.705C= MANE Select | NP_443106.1:p.Asn235= |