Linked Data
MyVariant Identifiers:
chr1:g.15772103T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445608T>G , CM000663.2:g.15445608T>G | GRCh38 |
| NC_000001.10:g.15772103T>G , CM000663.1:g.15772103T>G | GRCh37 |
| NC_000001.9:g.15644690T>G | NCBI36 |
| NG_009253.1:g.12166T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.651T>G MANE Select | ENSP00000365116.4:p.Gly217= | |
| ENST00000375943.6:c.*105T>G | ENSP00000365110.2:n.*105T>G | |
| ENST00000375949.4:c.651T>G | ENSP00000365116.4:p.Gly217= | |
| ENST00000483406.1:n.415T>G | ||
| NM_007272.2:c.651T>G | NP_009203.2:p.Gly217= | |
| XM_011540550.1:c.505T>G | XP_011538852.1:p.Trp169Gly | |
| NM_007272.3:c.651T>G MANE Select | NP_009203.2:p.Gly217= |