HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665868T>C , CM000679.2:g.39665868T>C | GRCh38 |
NC_000017.10:g.37822121T>C , CM000679.1:g.37822121T>C | GRCh37 |
NC_000017.9:g.35075647T>C | NCBI36 |
NG_008892.1:g.5523T>C , LRG_210:g.5523T>C | |
NG_042278.1:g.2888T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.263T>C MANE Select | ENSP00000312624.2:p.Val88Ala | |
ENST00000309889.2:c.263T>C | ENSP00000312624.2:p.Val88Ala | |
ENST00000578283.1:c.191T>C | ENSP00000462787.1:p.Val64Ala | |
NM_003673.3:c.263T>C , LRG_210t1:c.263T>C | NP_003664.1:p.Val88Ala | |
NM_003673.4:c.263T>C MANE Select | NP_003664.1:p.Val88Ala |