HGVS | Genome Assembly |
---|---|
NC_000008.11:g.117835485T= , CM000670.2:g.117835485T= | GRCh38 |
NC_000008.10:g.118847724T= , CM000670.1:g.118847724T= | GRCh37 |
NC_000008.9:g.118916905T= | NCBI36 |
NG_007455.2:g.281335A= , LRG_493:g.281335A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684189.1:n.590A= | ||
ENST00000378204.7:c.1123A= MANE Select | ENSP00000367446.3:p.Asn375= | |
ENST00000436216.2:c.491A= | ||
ENST00000378204.6:c.1123A= | ENSP00000367446.2:p.Asn375= | |
ENST00000436216.1:c.491A= | ||
ENST00000437196.1:c.*14A= | ENSP00000407299.1:n.*14A= | |
NM_000127.2:c.1123A= , LRG_493t1:c.1123A= | NP_000118.2:p.Asn375= | |
NM_000127.3:c.1123A= MANE Select | NP_000118.2:p.Asn375= |