HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48494251G= , CM000677.2:g.48494251G= | GRCh38 |
NC_000015.9:g.48786448G= , CM000677.1:g.48786448G= | GRCh37 |
NC_000015.8:g.46573740G= | NCBI36 |
NG_008805.2:g.156538C= , LRG_778:g.156538C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.2681C= | ENSP00000453958.2:p.Pro894= | |
ENST00000674301.2:c.2681C= | ENSP00000501333.2:p.Pro894= | |
ENST00000684448.1:n.1355C= | ||
ENST00000316623.10:c.2681C= MANE Select | ENSP00000325527.5:p.Pro894= | |
ENST00000316623.9:c.2681C= | ENSP00000325527.5:p.Pro894= | |
ENST00000537463.6:c.637-19601C= | ENSP00000440294.2:n.637-19601C= | |
NM_000138.4:c.2681C= , LRG_778t1:c.2681C= | NP_000129.3:p.Pro894= | |
NM_000138.5:c.2681C= MANE Select | NP_000129.3:p.Pro894= |