Linked Data
dbSNP Id:
rs761837484
ExAC:
15:75189403 C / T
gnomAD v2:
15-75189403-C-T
gnomAD v4:
15-74897062-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74897062C>T , CM000677.2:g.74897062C>T | GRCh38 |
| NC_000015.9:g.75189403C>T , CM000677.1:g.75189403C>T | GRCh37 |
| NC_000015.8:g.72976456C>T | NCBI36 |
| NG_008921.1:g.11994C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000352410.9:c.896C>T MANE Select | ENSP00000318318.6:p.Thr299Ile | |
| ENST00000323744.10:c.713C>T | ENSP00000318192.6:p.Thr238Ile | |
| ENST00000352410.8:c.896C>T | ENSP00000318318.6:p.Thr299Ile | |
| ENST00000535694.5:c.746C>T | ENSP00000440447.1:p.Thr249Ile | |
| ENST00000562800.5:c.256-477C>T | ENSP00000457619.1:n.256-477C>T | |
| ENST00000563786.5:c.836C>T | ENSP00000455241.1:p.Thr279Ile | |
| ENST00000566377.5:c.845-450C>T | ENSP00000455405.1:n.845-450C>T | |
| ENST00000566556.1:n.1629C>T | ||
| ENST00000567177.1:c.623-450C>T | ENSP00000457013.1:n.623-450C>T | |
| ENST00000569931.5:c.836C>T | ENSP00000455161.1:p.Thr279Ile | |
| NM_001289155.1:c.845-450C>T | NP_001276084.1:n.845-450C>T | |
| NM_001289156.1:c.746C>T | NP_001276085.1:p.Thr249Ile | |
| NM_001289157.1:c.713C>T | NP_001276086.1:p.Thr238Ile | |
| NM_002435.2:c.896C>T | NP_002426.1:p.Thr299Ile | |
| XM_011521592.1:c.884C>T | XP_011519894.1:p.Thr295Ile | |
| XM_011521593.1:c.836C>T | XP_011519895.1:p.Thr279Ile | |
| NM_001330372.1:c.836C>T | NP_001317301.1:p.Thr279Ile | |
| XM_017022208.1:c.785-450C>T | XP_016877697.1:n.785-450C>T | |
| XM_017022209.2:c.695-450C>T | XP_016877698.1:n.695-450C>T | |
| NM_002435.3:c.896C>T MANE Select | NP_002426.1:p.Thr299Ile | |
| NM_001289155.2:c.845-450C>T | NP_001276084.1:n.845-450C>T | |
| NM_001289156.2:c.746C>T | NP_001276085.1:p.Thr249Ile | |
| NM_001289157.2:c.713C>T | NP_001276086.1:p.Thr238Ile | |
| NM_001330372.2:c.836C>T | NP_001317301.1:p.Thr279Ile |