HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022630T= , CM000663.2:g.17022630T= | GRCh38 |
NC_000001.10:g.17349125T= , CM000663.1:g.17349125T= | GRCh37 |
NC_000001.9:g.17221712T= | NCBI36 |
NG_012340.1:g.36541A= , LRG_316:g.36541A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.572A= | ENSP00000481376.2:p.Asn191= | |
ENST00000491274.6:c.701A= | ENSP00000480482.2:p.Asn234= | |
ENST00000375499.8:c.743A= MANE Select | ENSP00000364649.3:p.Asn248= | |
ENST00000375499.7:c.743A= | ENSP00000364649.3:p.Asn248= | |
ENST00000475049.5:n.168A= | ||
ENST00000485092.5:n.407A= | ||
ENST00000485515.5:n.677A= | ||
NM_003000.2:c.743A= , LRG_316t1:c.743A= | NP_002991.2:p.Asn248= | |
NM_003000.3:c.743A= MANE Select | NP_002991.2:p.Asn248= |