HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107675113A>T , CM000669.2:g.107675113A>T | GRCh38 |
NC_000007.13:g.107315558A>T , CM000669.1:g.107315558A>T | GRCh37 |
NC_000007.12:g.107102794A>T | NCBI36 |
NG_008489.1:g.19479A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.765+4A>T MANE Select | ENSP00000494017.1:n.765+4A>T | |
ENST00000265715.7:c.765+4A>T | ENSP00000265715.3:n.765+4A>T | |
NM_000441.1:c.765+4A>T | NP_000432.1:n.765+4A>T | |
XM_005250425.1:c.765+4A>T | XP_005250482.1:n.765+4A>T | |
XM_006716025.2:c.765+4A>T | XP_006716088.1:n.765+4A>T | |
XM_005250425.2:c.765+4A>T | XP_005250482.1:n.765+4A>T | |
XM_006716025.3:c.765+4A>T | XP_006716088.1:n.765+4A>T | |
XM_017012318.1:c.765+4A>T | XP_016867807.1:n.765+4A>T | |
NM_000441.2:c.765+4A>T MANE Select | NP_000432.1:n.765+4A>T |