Linked Data
MyVariant Identifiers:
chr1:g.17349202G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022707G>T , CM000663.2:g.17022707G>T | GRCh38 |
| NC_000001.10:g.17349202G>T , CM000663.1:g.17349202G>T | GRCh37 |
| NC_000001.9:g.17221789G>T | NCBI36 |
| NG_012340.1:g.36464C>A , LRG_316:g.36464C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.495C>A | ENSP00000481376.2:p.Ser165= | |
| ENST00000491274.6:c.624C>A | ENSP00000480482.2:p.Ser208= | |
| ENST00000375499.8:c.666C>A MANE Select | ENSP00000364649.3:p.Ser222= | |
| ENST00000375499.7:c.666C>A | ENSP00000364649.3:p.Ser222= | |
| ENST00000475049.5:n.91C>A | ||
| ENST00000485092.5:n.330C>A | ||
| ENST00000485515.5:n.600C>A | ||
| NM_003000.2:c.666C>A , LRG_316t1:c.666C>A | NP_002991.2:p.Ser222= | |
| NM_003000.3:c.666C>A MANE Select | NP_002991.2:p.Ser222= |