MyVariant.info:
GRCh37
chr1:g.197396768A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197427638A>G , CM000663.2:g.197427638A>G | GRCh38 |
| NC_000001.10:g.197396768A>G , CM000663.1:g.197396768A>G | GRCh37 |
| NC_000001.9:g.195663391A>G | NCBI36 |
| NG_008483.1:g.164361A>G | |
| NG_008483.2:g.231177A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.2313A>G MANE Select | ENSP00000356370.3:p.Arg771= | |
| ENST00000638467.1:c.2313A>G | ENSP00000491102.1:p.Arg771= | |
| ENST00000681519.1:c.1194A>G | ENSP00000505267.1:p.Arg398= | |
| ENST00000367397.1:c.456A>G | ENSP00000356367.1:p.Arg152= | |
| ENST00000367399.6:c.1977A>G | ENSP00000356369.2:p.Arg659= | |
| ENST00000367400.7:c.2313A>G | ENSP00000356370.3:p.Arg771= | |
| ENST00000480086.2:n.214A>G | ||
| ENST00000484075.5:c.2313A>G | ENSP00000433932.1:p.Arg771= | |
| ENST00000535699.5:c.2106A>G | ENSP00000438786.1:p.Arg702= | |
| ENST00000538660.5:c.2128+5682A>G | ENSP00000438091.1:n.2128+5682A>G | |
| NM_001193640.1:c.1977A>G | NP_001180569.1:p.Arg659= | |
| NM_001257965.1:c.2106A>G | NP_001244894.1:p.Arg702= | |
| NM_001257966.1:c.2128+5682A>G | NP_001244895.1:n.2128+5682A>G | |
| NM_201253.2:c.2313A>G | NP_957705.1:p.Arg771= | |
| NR_047563.1:n.2314A>G | ||
| NR_047564.1:n.2522A>G | ||
| XM_011509365.1:c.2313A>G | XP_011507667.1:p.Arg771= | |
| XM_011509366.1:c.2313A>G | XP_011507668.1:p.Arg771= | |
| XM_011509367.1:c.2313A>G | XP_011507669.1:p.Arg771= | |
| XM_011509368.1:c.1731A>G | XP_011507670.1:p.Arg577= | |
| XM_011509369.1:c.756A>G | XP_011507671.1:p.Arg252= | |
| XM_011509365.2:c.2313A>G | XP_011507667.1:p.Arg771= | |
| XM_011509369.2:c.756A>G | XP_011507671.1:p.Arg252= | |
| XM_017000851.1:c.1470A>G | XP_016856340.1:p.Arg490= | |
| XM_017000852.1:c.2313A>G | XP_016856341.1:p.Arg771= | |
| NM_201253.3:c.2313A>G MANE Select | NP_957705.1:p.Arg771= | |
| NM_001193640.2:c.1977A>G | NP_001180569.1:p.Arg659= | |
| NM_001257965.2:c.2106A>G | NP_001244894.1:p.Arg702= | |
| NR_047563.2:n.2266A>G | ||
| NR_047564.2:n.2474A>G | ||
| NM_001257966.2:c.2128+5682A>G | NP_001244895.1:n.2128+5682A>G |