Linked Data
MyVariant Identifiers:
chr6:g.87725547C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.87015829C>G , CM000668.2:g.87015829C>G | GRCh38 |
| NC_000006.11:g.87725547C>G , CM000668.1:g.87725547C>G | GRCh37 |
| NC_000006.10:g.87782266C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305344.7:c.495C>G MANE Select | ENSP00000307766.4:p.Arg165= | |
| ENST00000305344.6:c.495C>G | ENSP00000307766.4:p.Arg165= | |
| NM_000865.2:c.495C>G | NP_000856.1:p.Arg165= | |
| XM_011535789.1:c.495C>G | XP_011534091.1:p.Arg165= | |
| XM_011535790.1:c.495C>G | XP_011534092.1:p.Arg165= | |
| XM_011535789.2:c.495C>G | XP_011534091.1:p.Arg165= | |
| NM_000865.3:c.495C>G MANE Select | NP_000856.1:p.Arg165= |