HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48468433G= , CM000677.2:g.48468433G= | GRCh38 |
NC_000015.9:g.48760630G= , CM000677.1:g.48760630G= | GRCh37 |
NC_000015.8:g.46547922G= | NCBI36 |
NG_008805.2:g.182356C= , LRG_778:g.182356C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4561C= | ENSP00000453958.2:p.Pro1521= | |
ENST00000674301.2:c.4561C= | ENSP00000501333.2:p.Pro1521= | |
ENST00000684448.1:n.3235C= | ||
ENST00000316623.10:c.4561C= MANE Select | ENSP00000325527.5:p.Pro1521= | |
ENST00000316623.9:c.4561C= | ENSP00000325527.5:p.Pro1521= | |
ENST00000537463.6:c.*324C= | ENSP00000440294.2:n.*324C= | |
NM_000138.4:c.4561C= , LRG_778t1:c.4561C= | NP_000129.3:p.Pro1521= | |
NM_000138.5:c.4561C= MANE Select | NP_000129.3:p.Pro1521= |