Linked Data
gnomAD v4:
2-176118937-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176118937C>T , CM000664.2:g.176118937C>T | GRCh38 |
| NC_000002.11:g.176983665C>T , CM000664.1:g.176983665C>T | GRCh37 |
| NC_000002.10:g.176691911C>T | NCBI36 |
| NG_008133.2:g.12174C>T , LRG_246:g.12174C>T | |
| NG_009225.1:g.1253C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249501.5:c.746-17C>T MANE Select | ENSP00000249501.4:n.746-17C>T | |
| ENST00000249501.4:c.746-17C>T | ENSP00000249501.4:n.746-17C>T | |
| ENST00000490088.2:n.570-17C>T | ||
| ENST00000549469.1:n.617-17C>T | ||
| NM_002148.3:c.746-17C>T , LRG_246t1:c.746-17C>T | NP_002139.2:n.746-17C>T | |
| NM_002148.4:c.746-17C>T MANE Select | NP_002139.2:n.746-17C>T |