MyVariant.info:
GRCh37
chr10:g.101964874T>C
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100205117T>C , CM000672.2:g.100205117T>C | GRCh38 |
| NC_000010.10:g.101964874T>C , CM000672.1:g.101964874T>C | GRCh37 |
| NC_000010.9:g.101954864T>C | NCBI36 |
| NG_028023.1:g.29471A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370397.8:c.1314A>G MANE Select | ENSP00000359424.6:p.Lys438= | |
| ENST00000370397.7:c.1314A>G | ENSP00000359424.6:p.Lys438= | |
| NM_001278.3:c.1314A>G | NP_001269.3:p.Lys438= | |
| XM_011539196.1:c.1314A>G | XP_011537498.1:p.Lys438= | |
| XM_011539197.1:c.1314A>G | XP_011537499.1:p.Lys438= | |
| XM_011539198.1:c.1314A>G | XP_011537500.1:p.Lys438= | |
| XR_945589.1:n.1392A>G | ||
| XR_945590.1:n.1289A>G | ||
| NM_001278.4:c.1314A>G | NP_001269.3:p.Lys438= | |
| NM_001320928.1:c.1314A>G | NP_001307857.1:p.Lys438= | |
| XM_017015611.1:c.1314A>G | XP_016871100.1:p.Lys438= | |
| XM_017015612.1:c.1314A>G | XP_016871101.1:p.Lys438= | |
| XM_017015613.1:c.102A>G | XP_016871102.1:p.Lys34= | |
| XR_001747010.1:n.1392A>G | ||
| XR_001747011.1:n.1289A>G | ||
| NM_001278.5:c.1314A>G MANE Select | NP_001269.3:p.Lys438= | |
| NM_001320928.2:c.1314A>G | NP_001307857.1:p.Lys438= |