HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112228649A= , CM000673.2:g.112228649A= | GRCh38 |
NC_000011.9:g.112099372A= , CM000673.1:g.112099372A= | GRCh37 |
NC_000011.8:g.111604582A= | NCBI36 |
NG_008743.1:g.7285A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000280362.8:c.139A= MANE Select | ENSP00000280362.3:p.Asn47= | |
ENST00000280362.7:c.139A= | ENSP00000280362.3:p.Asn47= | |
ENST00000524931.1:c.-66A= | ENSP00000434688.1:n.-66A= | |
ENST00000525645.1:n.214A= | ||
ENST00000525803.1:c.139A= | ENSP00000431750.1:p.Asn47= | |
ENST00000528679.5:c.139A= | ENSP00000435895.1:p.Asn47= | |
ENST00000531673.5:c.139A= | ENSP00000433469.1:p.Asn47= | |
NM_000317.2:c.139A= | NP_000308.1:p.Asn47= | |
NM_000317.3:c.139A= MANE Select | NP_000308.1:p.Asn47= |