HGVS | Genome Assembly |
---|---|
NC_000002.12:g.71124378A>G , CM000664.2:g.71124378A>G | GRCh38 |
NC_000002.11:g.71351508A>G , CM000664.1:g.71351508A>G | GRCh37 |
NC_000002.10:g.71205016A>G | NCBI36 |
NG_008977.1:g.10887T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000244217.6:c.206T>C MANE Select | ENSP00000244217.5:p.Leu69Pro | |
ENST00000244217.5:c.206T>C | ENSP00000244217.5:p.Leu69Pro | |
ENST00000413592.5:c.74T>C | ENSP00000391140.1:p.Leu25Pro | |
ENST00000486135.1:c.-80T>C | ENSP00000441569.1:n.-80T>C | |
ENST00000494660.6:c.-80T>C | ENSP00000437361.1:n.-80T>C | |
NM_032601.3:c.206T>C | NP_115990.3:p.Leu69Pro | |
XM_005264613.2:c.206T>C | XP_005264670.1:p.Leu69Pro | |
XR_939729.1:n.275T>C | ||
XR_939729.2:n.275T>C | ||
NM_032601.4:c.206T>C MANE Select | NP_115990.3:p.Leu69Pro |