HGVS | Genome Assembly |
---|---|
NC_000012.12:g.14507250T>C , CM000674.2:g.14507250T>C | GRCh38 |
NC_000012.11:g.14660184T>C , CM000674.1:g.14660184T>C | GRCh37 |
NC_000012.10:g.14551451T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000240617.10:c.1187-132A>G MANE Select | ENSP00000240617.5:n.1187-132A>G | |
ENST00000240617.9:c.1187-132A>G | ENSP00000240617.5:n.1187-132A>G | |
NM_024829.5:c.1187-132A>G | NP_079105.4:n.1187-132A>G | |
NM_024829.6:c.1187-132A>G MANE Select | NP_079105.4:n.1187-132A>G |