MyVariant.info:
GRCh37
chr4:g.100239327T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99318170T>C , CM000666.2:g.99318170T>C | GRCh38 |
| NC_000004.11:g.100239327T>C , CM000666.1:g.100239327T>C | GRCh37 |
| NC_000004.10:g.100458350T>C | NCBI36 |
| NG_011435.1:g.8246A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305046.13:c.135A>G MANE Select | ENSP00000306606.8:p.Gly45= | |
| ENST00000639454.1:c.135A>G | ENSP00000491622.1:p.Gly45= | |
| ENST00000305046.12:c.135A>G | ENSP00000306606.8:p.Gly45= | |
| ENST00000504498.1:n.189A>G | ||
| ENST00000506651.5:c.15A>G | ENSP00000425998.2:p.Gly5= | |
| ENST00000515694.4:n.2230A>G | ||
| ENST00000625860.2:c.15A>G | ENSP00000486614.1:p.Gly5= | |
| ENST00000632775.1:n.698A>G | ||
| NM_000668.5:c.135A>G | NP_000659.2:p.Gly45= | |
| NM_001286650.1:c.15A>G | NP_001273579.1:p.Gly5= | |
| NM_000668.6:c.135A>G MANE Select | NP_000659.2:p.Gly45= | |
| NM_001286650.2:c.15A>G | NP_001273579.1:p.Gly5= |