HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135851192A= , CM000664.2:g.135851192A= | GRCh38 |
NC_000002.11:g.136608762A= , CM000664.1:g.136608762A= | GRCh37 |
NC_000002.10:g.136325232A= | NCBI36 |
NG_008104.2:g.8978T= , LRG_338:g.8978T= | |
NG_008958.1:g.30250T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264156.3:c.1917+210T= MANE Select | ENSP00000264156.2:n.1917+210T= | |
ENST00000264156.2:c.1917+210T= | ENSP00000264156.2:n.1917+210T= | |
ENST00000483902.1:n.544+210T= | ||
ENST00000492091.1:n.343+210T= | ||
NM_005915.5:c.1917+210T= | NP_005906.2:n.1917+210T= | |
NM_005915.6:c.1917+210T= MANE Select | NP_005906.2:n.1917+210T= |