HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19589556A>G , CM000686.2:g.19589556A>G | GRCh38 |
NC_000024.9:g.21751442A>G , CM000686.1:g.21751442A>G | GRCh37 |
NC_000024.8:g.20210830A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000686158.1:n.533A>G | ||
ENST00000686905.1:n.1618A>G | ||
ENST00000693214.1:n.1706A>G | ||
ENST00000445715.6:n.435A>G | ||
ENST00000407724.7:n.779A>G | ||
ENST00000445715.5:n.435A>G | ||
ENST00000447202.2:n.2470A>G | ||
ENST00000447520.5:n.435A>G | ||
ENST00000459719.6:n.1706A>G | ||
ENST00000538014.2:n.1725A>G | ||
ENST00000585549.5:n.78A>G | ||
ENST00000587095.1:n.76A>G | ||
ENST00000588613.5:n.144A>G | ||
ENST00000589075.5:n.117A>G | ||
NR_045128.1:n.459A>G | ||
NR_045129.1:n.459A>G |