HGVS | Genome Assembly |
---|---|
NC_000020.11:g.45547426A>G , CM000682.2:g.45547426A>G | GRCh38 |
NC_000020.10:g.44176065A>G , CM000682.1:g.44176065A>G | GRCh37 |
NC_000020.9:g.43609479A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651288.1:c.-69T>C (EPPIN-WFDC6) | ENSP00000498632.1:n.-69T>C | |
ENST00000409554.1:c.-69T>C (EPPIN) | ENSP00000387153.1:n.-69T>C | |
ENST00000504988.1:c.-69T>C (EPPIN-WFDC6) | ENSP00000424176.1:n.-69T>C | |
NM_001198986.1:c.-69T>C (EPPIN-WFDC6) | NP_001185915.1:n.-69T>C | |
NM_001302861.1:c.-69T>C (EPPIN) | NP_001289790.1:n.-69T>C | |
NM_020398.3:c.-69T>C (EPPIN) | NP_065131.1:n.-69T>C |