HGVS | Genome Assembly |
---|---|
NC_000023.11:g.71223702G= , CM000685.2:g.71223702G= | GRCh38 |
NC_000023.10:g.70443552G= , CM000685.1:g.70443552G= | GRCh37 |
NC_000023.9:g.70360277G= | NCBI36 |
NG_008357.1:g.13491G= , LRG_245:g.13491G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361726.7:c.-6G= MANE Select | ENSP00000354900.6:n.-6G= | |
ENST00000374029.2:c.-6G= | ENSP00000363141.1:n.-6G= | |
ENST00000447581.2:c.-6G= | ENSP00000407223.2:n.-6G= | |
ENST00000645009.2:c.-6G= | ENSP00000494142.2:n.-6G= | |
ENST00000646835.1:c.-6G= | ENSP00000494596.1:n.-6G= | |
ENST00000647424.1:c.-6G= | ENSP00000495960.1:n.-6G= | |
ENST00000674549.1:c.-6G= | ENSP00000502766.1:n.-6G= | |
ENST00000674844.1:c.-6G= | ENSP00000502556.1:n.-6G= | |
ENST00000675209.1:c.-6G= | ENSP00000501813.1:n.-6G= | |
ENST00000675368.1:c.-6G= | ENSP00000501757.1:n.-6G= | |
ENST00000675609.1:c.-6G= | ENSP00000501571.1:n.-6G= | |
ENST00000361726.6:c.-6G= | ENSP00000354900.6:n.-6G= | |
ENST00000374022.3:c.-6G= | ENSP00000363134.3:n.-6G= | |
ENST00000374029.1:c.-6G= | ENSP00000363141.1:n.-6G= | |
ENST00000447581.1:c.-6G= | ENSP00000407223.1:n.-6G= | |
NM_000166.5:c.-6G= | NP_000157.1:n.-6G= | |
NM_001097642.2:c.-6G= , LRG_245t1:c.-6G= | NP_001091111.1:n.-6G= | |
XM_011530907.1:c.-6G= | XP_011529209.1:n.-6G= | |
XM_011530907.2:c.-6G= | XP_011529209.1:n.-6G= | |
NM_000166.6:c.-6G= MANE Select | NP_000157.1:n.-6G= | |
NM_001097642.3:c.-6G= | NP_001091111.1:n.-6G= |