HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160489485T>A , CM000668.2:g.160489485T>A | GRCh38 |
NC_000006.11:g.160910517T>A , CM000668.1:g.160910517T>A | GRCh37 |
NC_000006.10:g.160830507T>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000454031.6:n.549+1878A>T | ||
ENST00000335388.5:n.509-2053A>T | ||
ENST00000435757.6:n.509-2053A>T | ||
ENST00000454031.5:n.549+1878A>T | ||
NR_028092.1:n.509-2053A>T | ||
NR_028093.1:n.509-2053A>T | ||
XR_943184.1:n.458+1443T>A | ||
XR_943185.1:n.458+1443T>A | ||
XR_943186.1:n.515+1443T>A |