HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19589385A>C , CM000686.2:g.19589385A>C | GRCh38 |
NC_000024.9:g.21751271A>C , CM000686.1:g.21751271A>C | GRCh37 |
NC_000024.8:g.20210659A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686158.1:n.498-136A>C | ||
ENST00000686905.1:n.1447A>C | ||
ENST00000693214.1:n.1535A>C | ||
ENST00000445715.6:n.400-136A>C | ||
ENST00000407724.7:n.750-142A>C | ||
ENST00000445715.5:n.400-136A>C | ||
ENST00000447202.2:n.2299A>C | ||
ENST00000447520.5:n.400-136A>C | ||
ENST00000459719.6:n.1535A>C | ||
ENST00000538014.2:n.1554A>C | ||
ENST00000585549.5:n.43-136A>C | ||
ENST00000587095.1:n.41-136A>C | ||
ENST00000588613.5:n.109-136A>C | ||
ENST00000589075.5:n.82-136A>C | ||
NR_045128.1:n.424-136A>C | ||
NR_045129.1:n.424-136A>C |