Linked Data
MyVariant Identifiers:
chr1:g.161559627C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161589837C>G , CM000663.2:g.161589837C>G | GRCh38 |
| NC_000001.10:g.161559627C>G , CM000663.1:g.161559627C>G | GRCh37 |
| NC_000001.9:g.159826251C>G | NCBI36 |
| NG_011982.1:g.13499C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699402.1:c.41-40806G>C | ENSP00000514363.1:n.41-40806G>C | |
| ENST00000699403.1:c.61+40531G>C | ENSP00000514364.1:n.61+40531G>C | |
| ENST00000465075.6:n.483+18C>G | ||
| ENST00000466542.6:c.391+18C>G | ENSP00000426627.1:n.391+18C>G | |
| ENST00000473530.6:n.572+18C>G | ||
| ENST00000473712.6:n.413+18C>G | ||
| ENST00000482226.2:n.370+18C>G | ||
| ENST00000496692.6:n.505C>G | ||
| ENST00000543859.5:c.388+18C>G | ENSP00000444663.2:n.388+18C>G | |
| ENST00000611236.1:c.388+18C>G | ENSP00000480953.1:n.388+18C>G | |
| NR_047648.1:n.490+18C>G |