HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64751695C>A , CM000673.2:g.64751695C>A | GRCh38 |
NC_000011.9:g.64519167C>A , CM000673.1:g.64519167C>A | GRCh37 |
NC_000011.8:g.64275743C>A | NCBI36 |
NG_013018.1:g.14021G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.1769-40G>T MANE Select | ENSP00000164139.3:n.1769-40G>T | |
ENST00000164139.3:c.1769-40G>T | ENSP00000164139.3:n.1769-40G>T | |
ENST00000377432.7:c.1505-40G>T | ENSP00000366650.3:n.1505-40G>T | |
ENST00000462303.1:n.93-40G>T | ||
NM_001164716.1:c.1505-40G>T | NP_001158188.1:n.1505-40G>T | |
NM_005609.2:c.1769-40G>T | NP_005600.1:n.1769-40G>T | |
NM_005609.3:c.1769-40G>T | NP_005600.1:n.1769-40G>T | |
NM_005609.4:c.1769-40G>T MANE Select | NP_005600.1:n.1769-40G>T |