HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154997085A>T , CM000685.2:g.154997085A>T | GRCh38 |
NC_000023.10:g.154225360A>T , CM000685.1:g.154225360A>T | GRCh37 |
NC_000023.9:g.153878554A>T | NCBI36 |
NG_011403.1:g.30639T>A | |
NG_011403.2:g.30639T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.276T>A MANE Select | ENSP00000353393.4:p.Gly92= | |
ENST00000647125.1:c.*62T>A | ENSP00000496062.1:n.*62T>A | |
ENST00000360256.8:c.276T>A | ENSP00000353393.4:p.Gly92= | |
ENST00000423959.5:c.171T>A | ENSP00000409446.1:p.Gly57= | |
ENST00000453950.1:c.258T>A | ENSP00000389153.1:p.Gly86= | |
NM_000132.3:c.276T>A | NP_000123.1:p.Gly92= | |
XM_011531126.1:c.171T>A | XP_011529428.1:p.Gly57= | |
NM_000132.4:c.276T>A MANE Select | NP_000123.1:p.Gly92= |