HGVS | Genome Assembly |
---|---|
NC_000005.10:g.150860568T>C , CM000667.2:g.150860568T>C | GRCh38 |
NC_000005.9:g.150240130T>C , CM000667.1:g.150240130T>C | GRCh37 |
NC_000005.8:g.150220323T>C | NCBI36 |
NG_027809.2:g.19046T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000520549.1:c.158+11914T>C | ||
XM_011537641.1:c.531+11914T>C | XP_011535943.1:n.531+11914T>C | |
NM_001346557.1:c.531+11914T>C | NP_001333486.1:n.531+11914T>C | |
NM_001346557.2:c.531+11914T>C | NP_001333486.1:n.531+11914T>C | |
NR_170598.1:n.1646+11914T>C |