HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19939303T>C , CM000670.2:g.19939303T>C | GRCh38 |
NC_000008.10:g.19796814T>C , CM000670.1:g.19796814T>C | GRCh37 |
NC_000008.9:g.19841094T>C | NCBI36 |
NG_008855.1:g.5233T>C | |
NG_008855.2:g.42587T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.-138T>C MANE Select | ENSP00000497642.1:n.-138T>C | |
ENST00000311322.8:c.-138T>C | ENSP00000309757.6:n.-138T>C | |
ENST00000519773.1:c.-138T>C | ENSP00000431028.1:n.-138T>C | |
ENST00000520959.5:c.-140-8877T>C | ENSP00000428496.1:n.-140-8877T>C | |
ENST00000521994.1:n.48T>C | ||
ENST00000522701.5:c.-138T>C | ENSP00000428557.1:n.-138T>C | |
ENST00000524029.5:c.-138T>C | ENSP00000428237.1:n.-138T>C | |
NM_000237.2:c.-138T>C | NP_000228.1:n.-138T>C | |
NM_000237.3:c.-138T>C MANE Select | NP_000228.1:n.-138T>C |