Linked Data
MyVariant Identifiers:
chr8:g.37823727T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966209T>C , CM000670.2:g.37966209T>C | GRCh38 |
| NC_000008.10:g.37823727T>C , CM000670.1:g.37823727T>C | GRCh37 |
| NC_000008.9:g.37942884T>C | NCBI36 |
| NG_011936.1:g.5458A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000345060.5:c.261A>G MANE Select | ENSP00000343782.3:p.Gly87= | |
| ENST00000520341.2:n.389A>G | ||
| ENST00000345060.4:c.261A>G | ENSP00000343782.3:p.Gly87= | |
| ENST00000614635.1:c.261A>G | ENSP00000480325.1:p.Gly87= | |
| NM_000025.2:c.261A>G | NP_000016.1:p.Gly87= | |
| NM_000025.3:c.261A>G MANE Select | NP_000016.1:p.Gly87= |