HGVS | Genome Assembly |
---|---|
NC_000009.12:g.98541597A= , CM000671.2:g.98541597A= | GRCh38 |
NC_000009.11:g.101303879A= , CM000671.1:g.101303879A= | GRCh37 |
NC_000009.10:g.100343700A= | NCBI36 |
NG_016426.1:g.172601T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259455.4:c.630+276T= MANE Select | ENSP00000259455.2:n.630+276T= | |
ENST00000637410.1:n.408+276T= | ||
ENST00000259455.3:c.630+276T= | ENSP00000259455.2:n.630+276T= | |
ENST00000477471.1:n.417+276T= | ||
ENST00000634227.1:n.404+276T= | ||
NM_005458.7:c.630+276T= | NP_005449.5:n.630+276T= | |
XM_017015331.2:c.336+276T= | XP_016870820.1:n.336+276T= | |
NM_005458.8:c.630+276T= MANE Select | NP_005449.5:n.630+276T= |