HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31622757A>G , CM000668.2:g.31622757A>G | GRCh38 |
NC_000006.11:g.31590534A>G , CM000668.1:g.31590534A>G | GRCh37 |
NC_000006.10:g.31698513A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376033.3:c.-33A>G MANE Select | ENSP00000365201.2:n.-33A>G | |
ENST00000376007.8:c.-33A>G | ENSP00000365175.4:n.-33A>G | |
ENST00000376033.2:c.-33A>G | ENSP00000365201.2:n.-33A>G | |
ENST00000469577.5:n.136-1504A>G | ||
NM_004638.3:c.-33A>G | NP_004629.3:n.-33A>G | |
NM_080686.2:c.-33A>G | NP_542417.2:n.-33A>G | |
XM_011514890.1:c.-33A>G | XP_011513192.1:n.-33A>G | |
NM_004638.4:c.-33A>G MANE Select | NP_004629.3:n.-33A>G | |
NM_080686.3:c.-33A>G | NP_542417.2:n.-33A>G |