MyVariant.info:
GRCh37
chr18:g.29111012T>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31531049T>G , CM000680.2:g.31531049T>G | GRCh38 |
| NC_000018.9:g.29111012T>G , CM000680.1:g.29111012T>G | GRCh37 |
| NC_000018.8:g.27365010T>G | NCBI36 |
| NG_007072.3:g.37808T>G , LRG_397:g.37808T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683614.2:n.908T>G | ||
| ENST00000683614.1:c.908T>G | ||
| ENST00000261590.13:c.1077T>G MANE Select | ENSP00000261590.8:p.Ala359= | |
| ENST00000261590.12:c.1077T>G | ENSP00000261590.8:p.Ala359= | |
| NM_001943.3:c.1077T>G , LRG_397t1:c.1077T>G | NP_001934.2:p.Ala359= | |
| NM_001943.4:c.1077T>G | NP_001934.2:p.Ala359= | |
| XM_024451095.1:c.543T>G | XP_024306863.1:p.Ala181= | |
| NM_001943.5:c.1077T>G MANE Select | NP_001934.2:p.Ala359= |