HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120739327T>C , CM000674.2:g.120739327T>C | GRCh38 |
NC_000012.11:g.121177130T>C , CM000674.1:g.121177130T>C | GRCh37 |
NC_000012.10:g.119661513T>C | NCBI36 |
NG_007991.1:g.18560T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000242592.9:c.1118T>C MANE Select | ENSP00000242592.4:p.Val373Ala | |
ENST00000242592.8:c.1118T>C | ENSP00000242592.4:p.Val373Ala | |
ENST00000411593.2:c.1106T>C | ENSP00000401045.2:p.Val369Ala | |
NM_000017.3:c.1118T>C | NP_000008.1:p.Val373Ala | |
NM_001302554.1:c.1106T>C | NP_001289483.1:p.Val369Ala | |
NM_000017.4:c.1118T>C MANE Select | NP_000008.1:p.Val373Ala | |
NM_001302554.2:c.1106T>C | NP_001289483.1:p.Val369Ala |