Linked Data
dbSNP Id:
rs1967961598
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713352G>A , CM000681.2:g.6713352G>A | GRCh38 |
| NC_000019.9:g.6713363G>A , CM000681.1:g.6713363G>A | GRCh37 |
| NC_000019.8:g.6664363G>A | NCBI36 |
| NG_009557.1:g.12300C>T , LRG_27:g.12300C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.754-37C>T | ENSP00000512083.1:n.754-37C>T | |
| ENST00000695692.1:n.201-37C>T | ||
| ENST00000245907.11:c.877-37C>T MANE Select | ENSP00000245907.4:n.877-37C>T | |
| ENST00000245907.10:c.877-37C>T | ENSP00000245907.4:n.877-37C>T | |
| ENST00000595577.1:n.381-37C>T | ||
| ENST00000597442.5:n.127-37C>T | ||
| NM_000064.3:c.877-37C>T | NP_000055.2:n.877-37C>T | |
| NM_000064.4:c.877-37C>T MANE Select | NP_000055.2:n.877-37C>T |