HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112228641A>T , CM000673.2:g.112228641A>T | GRCh38 |
NC_000011.9:g.112099364A>T , CM000673.1:g.112099364A>T | GRCh37 |
NC_000011.8:g.111604574A>T | NCBI36 |
NG_008743.1:g.7277A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000280362.8:c.131A>T MANE Select | ENSP00000280362.3:p.Asn44Ile | |
ENST00000280362.7:c.131A>T | ENSP00000280362.3:p.Asn44Ile | |
ENST00000524931.1:c.-74A>T | ENSP00000434688.1:n.-74A>T | |
ENST00000525645.1:n.206A>T | ||
ENST00000525803.1:c.131A>T | ENSP00000431750.1:p.Asn44Ile | |
ENST00000528679.5:c.131A>T | ENSP00000435895.1:p.Asn44Ile | |
ENST00000531673.5:c.131A>T | ENSP00000433469.1:p.Asn44Ile | |
NM_000317.2:c.131A>T | NP_000308.1:p.Asn44Ile | |
NM_000317.3:c.131A>T MANE Select | NP_000308.1:p.Asn44Ile |