HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19589564G= , CM000686.2:g.19589564G= | GRCh38 |
NC_000024.9:g.21751450G= , CM000686.1:g.21751450G= | GRCh37 |
NC_000024.8:g.20210838G= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000686158.1:n.541G= | ||
ENST00000686905.1:n.1626G= | ||
ENST00000693214.1:n.1714G= | ||
ENST00000445715.6:n.443G= | ||
ENST00000407724.7:n.787G= | ||
ENST00000445715.5:n.443G= | ||
ENST00000447202.2:n.2478G= | ||
ENST00000447520.5:n.443G= | ||
ENST00000459719.6:n.1714G= | ||
ENST00000538014.2:n.1733G= | ||
ENST00000585549.5:n.86G= | ||
ENST00000587095.1:n.84G= | ||
ENST00000588613.5:n.152G= | ||
ENST00000589075.5:n.125G= | ||
NR_045128.1:n.467G= | ||
NR_045129.1:n.467G= |