HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23425563T>C , CM000676.2:g.23425563T>C | GRCh38 |
NC_000014.8:g.23894772T>C , CM000676.1:g.23894772T>C | GRCh37 |
NC_000014.7:g.22964612T>C | NCBI36 |
NG_007884.1:g.15099A>G , LRG_384:g.15099A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2286+132A>G MANE Select | ENSP00000347507.3:n.2286+132A>G | |
ENST00000355349.3:c.2286+132A>G | ENSP00000347507.3:n.2286+132A>G | |
NM_000257.3:c.2286+132A>G | NP_000248.2:n.2286+132A>G | |
XR_245686.3:n.2392+132A>G | ||
XM_017021340.1:c.2286+132A>G | XP_016876829.1:n.2286+132A>G | |
NM_000257.4:c.2286+132A>G MANE Select | NP_000248.2:n.2286+132A>G |