HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43552262A>C , CM000681.2:g.43552262A>C | GRCh38 |
NC_000019.9:g.44056414A>C , CM000681.1:g.44056414A>C | GRCh37 |
NC_000019.8:g.48748254A>C | NCBI36 |
NG_033799.1:g.28317T>G , LRG_784:g.28317T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262887.10:c.837T>G MANE Select | ENSP00000262887.5:p.Thr279= | |
ENST00000262887.9:c.837T>G | ENSP00000262887.4:p.Thr279= | |
ENST00000543982.5:c.744T>G | ENSP00000443671.1:p.Thr248= | |
ENST00000595789.5:n.958T>G | ||
ENST00000597811.5:c.447T>G | ||
ENST00000598165.5:c.858T>G | ENSP00000470045.1:p.Thr286= | |
ENST00000598422.1:n.517T>G | ||
NM_006297.2:c.837T>G , LRG_784t1:c.837T>G | NP_006288.2:p.Thr279= | |
NM_006297.3:c.837T>G MANE Select | NP_006288.2:p.Thr279= |