Linked Data
MyVariant Identifiers:
chr7:g.21856312C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21816694C>G , CM000669.2:g.21816694C>G | GRCh38 |
| NC_000007.13:g.21856312C>G , CM000669.1:g.21856312C>G | GRCh37 |
| NC_000007.12:g.21822837C>G | NCBI36 |
| NG_012886.2:g.278480C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.10560C>G MANE Select | ENSP00000475939.1:p.Gly3520= | |
| ENST00000328843.10:c.10581C>G | ENSP00000330671.7:p.Gly3527= | |
| ENST00000409508.7:c.10560C>G | ENSP00000475939.1:p.Gly3520= | |
| ENST00000620169.4:c.10581C>G | ENSP00000481693.1:p.Gly3527= | |
| NM_001277115.1:c.10560C>G | NP_001264044.1:p.Gly3520= | |
| NM_001277115.2:c.10560C>G MANE Select | NP_001264044.1:p.Gly3520= |