HGVS | Genome Assembly |
---|---|
NC_000010.11:g.123040612T= , CM000672.2:g.123040612T= | GRCh38 |
NC_000010.10:g.124800128T= , CM000672.1:g.124800128T= | GRCh37 |
NC_000010.9:g.124790118T= | NCBI36 |
NG_008003.1:g.36700T= , LRG_451:g.36700T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000358776.7:c.450T= MANE Select | ENSP00000357873.3:p.Ile150= | |
ENST00000358776.6:c.450T= | ENSP00000357873.3:p.Ile150= | |
ENST00000368869.8:c.144T= | ENSP00000357862.4:p.Ile48= | |
ENST00000411816.2:n.467T= | ||
NM_001609.3:c.450T= , LRG_451t1:c.450T= | NP_001600.1:p.Ile150= | |
NM_001330174.1:c.144T= | NP_001317103.1:p.Ile48= | |
NM_001330174.2:c.144T= | NP_001317103.1:p.Ile48= | |
NM_001609.4:c.450T= MANE Select | NP_001600.1:p.Ile150= | |
NM_001330174.3:c.144T= | NP_001317103.1:p.Ile48= |