HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57562653C>A , CM000682.2:g.57562653C>A | GRCh38 |
NC_000020.10:g.56137709C>A , CM000682.1:g.56137709C>A | GRCh37 |
NC_000020.9:g.55571115C>A | NCBI36 |
NG_008205.1:g.6573C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.407-43C>A MANE Select | ENSP00000319814.4:n.407-43C>A | |
ENST00000319441.5:c.407-43C>A | ENSP00000319814.4:n.407-43C>A | |
ENST00000467047.1:n.1574C>A | ||
ENST00000498194.1:n.306C>A | ||
NM_002591.3:c.407-43C>A | NP_002582.3:n.407-43C>A | |
XM_011528839.1:c.11-43C>A | XP_011527141.1:n.11-43C>A | |
XM_024451888.1:c.11-43C>A | XP_024307656.1:n.11-43C>A | |
NM_002591.4:c.407-43C>A MANE Select | NP_002582.3:n.407-43C>A |