HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713314A>T , CM000681.2:g.6713314A>T | GRCh38 |
NC_000019.9:g.6713325A>T , CM000681.1:g.6713325A>T | GRCh37 |
NC_000019.8:g.6664325A>T | NCBI36 |
NG_009557.1:g.12338T>A , LRG_27:g.12338T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.755T>A | ENSP00000512083.1:p.Ile252Asn | |
ENST00000695654.1:c.2T>A | ENSP00000512085.1:p.Ile1Asn | |
ENST00000695692.1:n.202T>A | ||
ENST00000245907.11:c.878T>A MANE Select | ENSP00000245907.4:p.Ile293Asn | |
ENST00000245907.10:c.878T>A | ENSP00000245907.4:p.Ile293Asn | |
ENST00000594270.5:n.2T>A | ||
ENST00000595577.1:n.382T>A | ||
ENST00000597442.5:n.128T>A | ||
NM_000064.3:c.878T>A | NP_000055.2:p.Ile293Asn | |
NM_000064.4:c.878T>A MANE Select | NP_000055.2:p.Ile293Asn |