HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64752670A>G , CM000673.2:g.64752670A>G | GRCh38 |
NC_000011.9:g.64520142A>G , CM000673.1:g.64520142A>G | GRCh37 |
NC_000011.8:g.64276718A>G | NCBI36 |
NG_013018.1:g.13046T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.1519-166T>C MANE Select | ENSP00000164139.3:n.1519-166T>C | |
ENST00000164139.3:c.1519-166T>C | ENSP00000164139.3:n.1519-166T>C | |
ENST00000377432.7:c.1255-166T>C | ENSP00000366650.3:n.1255-166T>C | |
NM_001164716.1:c.1255-166T>C | NP_001158188.1:n.1255-166T>C | |
NM_005609.2:c.1519-166T>C | NP_005600.1:n.1519-166T>C | |
NM_005609.3:c.1519-166T>C | NP_005600.1:n.1519-166T>C | |
NM_005609.4:c.1519-166T>C MANE Select | NP_005600.1:n.1519-166T>C |