MyVariant.info:
GRCh37
chr1:g.155207261G>A
gnomAD v4:
Joint Max Group AF
0.00000183 (NFE)
Exomes Max Group AF
0.00000194 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155237470G>A , CM000663.2:g.155237470G>A | GRCh38 |
| NC_000001.10:g.155207261G>A , CM000663.1:g.155207261G>A | GRCh37 |
| NC_000001.9:g.153473885G>A | NCBI36 |
| NG_009783.1:g.12228C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368373.8:c.870C>T MANE Select | ENSP00000357357.3:p.Phe290= | |
| ENST00000327247.9:c.870C>T | ENSP00000314508.5:p.Phe290= | |
| ENST00000368373.7:c.870C>T | ENSP00000357357.3:p.Phe290= | |
| ENST00000427500.7:c.723C>T | ENSP00000402577.2:p.Phe241= | |
| ENST00000428024.3:c.609C>T | ENSP00000397986.2:p.Phe203= | |
| ENST00000484489.5:n.340-1182C>T | ||
| ENST00000491081.5:n.475C>T | ||
| ENST00000497670.5:n.493C>T | ||
| NM_000157.3:c.870C>T | NP_000148.2:p.Phe290= | |
| NM_001005741.2:c.870C>T | NP_001005741.1:p.Phe290= | |
| NM_001005742.2:c.870C>T | NP_001005742.1:p.Phe290= | |
| NM_001171811.1:c.609C>T | NP_001165282.1:p.Phe203= | |
| NM_001171812.1:c.723C>T | NP_001165283.1:p.Phe241= | |
| XM_006711270.1:c.870C>T | XP_006711333.1:p.Phe290= | |
| XM_011509407.1:c.870C>T | XP_011507709.1:p.Phe290= | |
| NM_000157.4:c.870C>T MANE Select | NP_000148.2:p.Phe290= | |
| NM_001005741.3:c.870C>T | NP_001005741.1:p.Phe290= | |
| NM_001005742.3:c.870C>T | NP_001005742.1:p.Phe290= | |
| NM_001171811.2:c.609C>T | NP_001165282.1:p.Phe203= | |
| NM_001171812.2:c.723C>T | NP_001165283.1:p.Phe241= |