HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022629G= , CM000663.2:g.17022629G= | GRCh38 |
NC_000001.10:g.17349124G= , CM000663.1:g.17349124G= | GRCh37 |
NC_000001.9:g.17221711G= | NCBI36 |
NG_012340.1:g.36542C= , LRG_316:g.36542C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.573C= | ENSP00000481376.2:p.Asn191= | |
ENST00000491274.6:c.702C= | ENSP00000480482.2:p.Asn234= | |
ENST00000375499.8:c.744C= MANE Select | ENSP00000364649.3:p.Asn248= | |
ENST00000375499.7:c.744C= | ENSP00000364649.3:p.Asn248= | |
ENST00000475049.5:n.169C= | ||
ENST00000485092.5:n.408C= | ||
ENST00000485515.5:n.678C= | ||
NM_003000.2:c.744C= , LRG_316t1:c.744C= | NP_002991.2:p.Asn248= | |
NM_003000.3:c.744C= MANE Select | NP_002991.2:p.Asn248= |