Linked Data
MyVariant Identifiers:
chr6:g.35773558C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35805781C>G , CM000668.2:g.35805781C>G | GRCh38 |
| NC_000006.11:g.35773558C>G , CM000668.1:g.35773558C>G | GRCh37 |
| NC_000006.10:g.35881536C>G | NCBI36 |
| NG_012184.1:g.5488C>G | |
| NG_012184.2:g.5488C>G | |
| NG_012184.3:g.13576C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360215.3:c.111C>G MANE Select | ENSP00000353346.1:p.Ser37= | |
| ENST00000651132.1:c.111C>G | ENSP00000498322.1:p.Ser37= | |
| ENST00000651676.1:c.111C>G | ENSP00000498699.1:p.Ser37= | |
| ENST00000651994.1:c.111C>G | ENSP00000498310.1:p.Ser37= | |
| ENST00000360215.2:c.111C>G | ENSP00000353346.1:p.Ser37= | |
| NM_182548.3:c.111C>G | NP_872354.1:p.Ser37= | |
| XM_011514403.1:c.111C>G | XP_011512705.1:p.Ser37= | |
| NM_182548.4:c.111C>G MANE Select | NP_872354.1:p.Ser37= |