HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17023915T= , CM000663.2:g.17023915T= | GRCh38 |
NC_000001.10:g.17350410T= , CM000663.1:g.17350410T= | GRCh37 |
NC_000001.9:g.17222997T= | NCBI36 |
NG_012340.1:g.35256A= , LRG_316:g.35256A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.471+58A= | ENSP00000481376.2:n.471+58A= | |
ENST00000491274.6:c.600+58A= | ENSP00000480482.2:n.600+58A= | |
ENST00000375499.8:c.642+58A= MANE Select | ENSP00000364649.3:n.642+58A= | |
ENST00000375499.7:c.642+58A= | ENSP00000364649.3:n.642+58A= | |
ENST00000485515.5:n.576+58A= | ||
NM_003000.2:c.642+58A= , LRG_316t1:c.642+58A= | NP_002991.2:n.642+58A= | |
NM_003000.3:c.642+58A= MANE Select | NP_002991.2:n.642+58A= |