HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80280312A>C , CM000672.2:g.80280312A>C | GRCh38 |
NC_000010.10:g.82040068A>C , CM000672.1:g.82040068A>C | GRCh37 |
NC_000010.9:g.82030048A>C | NCBI36 |
NG_008083.1:g.14367T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.410T>G MANE Select | ENSP00000361287.3:p.Leu137Trp | |
ENST00000372213.7:c.410T>G | ENSP00000361287.3:p.Leu137Trp | |
ENST00000455001.1:c.221T>G | ENSP00000414961.1:p.Leu74Trp | |
NM_000429.2:c.410T>G | NP_000420.1:p.Leu137Trp | |
XM_005269842.3:c.410T>G | XP_005269899.1:p.Leu137Trp | |
XM_005269843.3:c.287T>G | XP_005269900.1:p.Leu96Trp | |
NM_000429.3:c.410T>G MANE Select | NP_000420.1:p.Leu137Trp |