Linked Data
gnomAD v2:
14-74726515-G-GT
gnomAD v4:
14-74259812-G-GT
MyVariant Identifiers:
chr14:g.74726515_74726516insT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259812_74259813insT , CM000676.2:g.74259812_74259813insT | GRCh38 |
| NC_000014.8:g.74726515_74726516insT , CM000676.1:g.74726515_74726516insT | GRCh37 |
| NC_000014.7:g.73796268_73796269insT | NCBI36 |
| NG_013092.1:g.25341_25342insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.760+30_760+31insT MANE Select | ENSP00000261980.2:n.760+30_760+31insT | |
| ENST00000261980.2:c.760+30_760+31insT | ENSP00000261980.2:n.760+30_760+31insT | |
| NM_182894.2:c.760+30_760+31insT | NP_878314.1:n.760+30_760+31insT | |
| XM_011536719.1:c.760+30_760+31insT | XP_011535021.1:n.760+30_760+31insT | |
| NM_182894.3:c.760+30_760+31insT MANE Select | NP_878314.1:n.760+30_760+31insT |