HGVS | Genome Assembly |
---|---|
NC_000004.12:g.121696976A>G , CM000666.2:g.121696976A>G | GRCh38 |
NC_000004.11:g.122618131A>G , CM000666.1:g.122618131A>G | GRCh37 |
NC_000004.10:g.122837581A>G | NCBI36 |
NG_032042.1:g.5017T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000296511.10:c.-149T>C MANE Select | ENSP00000296511.5:n.-149T>C | |
ENST00000296511.9:c.-149T>C | ENSP00000296511.5:n.-149T>C | |
ENST00000509016.5:n.17T>C | ||
ENST00000513428.5:n.17T>C | ||
ENST00000513523.1:n.20T>C | ||
NM_001154.3:c.-149T>C | NP_001145.1:n.-149T>C | |
XM_017008141.2:c.-149T>C | XP_016863630.1:n.-149T>C | |
NM_001154.4:c.-149T>C MANE Select | NP_001145.1:n.-149T>C |