HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101421778G>C , CM000671.2:g.101421778G>C | GRCh38 |
NC_000009.11:g.104184060G>C , CM000671.1:g.104184060G>C | GRCh37 |
NC_000009.10:g.103223881G>C | NCBI36 |
NG_012387.1:g.19003C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647789.2:c.*31C>G MANE Select | ENSP00000497767.1:n.*31C>G | |
ENST00000648064.1:c.*31C>G | ENSP00000497990.1:n.*31C>G | |
ENST00000648758.1:c.*31C>G | ENSP00000497731.1:n.*31C>G | |
ENST00000374855.8:c.*31C>G | ENSP00000363988.4:n.*31C>G | |
ENST00000616752.1:c.*138C>G | ENSP00000481363.1:n.*138C>G | |
NM_000035.3:c.*31C>G | NP_000026.2:n.*31C>G | |
NM_000035.4:c.*31C>G MANE Select | NP_000026.2:n.*31C>G |