HGVS | Genome Assembly |
---|---|
NC_000004.12:g.121696981G>C , CM000666.2:g.121696981G>C | GRCh38 |
NC_000004.11:g.122618136G>C , CM000666.1:g.122618136G>C | GRCh37 |
NC_000004.10:g.122837586G>C | NCBI36 |
NG_032042.1:g.5012C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000296511.9:c.-154C>G | ENSP00000296511.5:n.-154C>G | |
ENST00000509016.5:n.12C>G | ||
ENST00000513428.5:n.12C>G | ||
ENST00000513523.1:n.15C>G | ||
NM_001154.3:c.-154C>G | NP_001145.1:n.-154C>G | |
XM_017008141.2:c.-154C>G | XP_016863630.1:n.-154C>G |