Linked Data
ClinVar Variation Id:
449251
ClinVar RCV Id:
RCV001821456
dbSNP Id:
rs150217523
ExAC:
15:75185070 G / A
gnomAD v2:
15-75185070-G-A
gnomAD v3:
15-74892729-G-A
gnomAD v4:
15-74892729-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74892729G>A , CM000677.2:g.74892729G>A | GRCh38 |
| NC_000015.9:g.75185070G>A , CM000677.1:g.75185070G>A | GRCh37 |
| NC_000015.8:g.72972123G>A | NCBI36 |
| NG_008921.1:g.7661G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000352410.9:c.414G>A MANE Select | ENSP00000318318.6:p.Met138Ile | |
| ENST00000323744.10:c.414G>A | ENSP00000318192.6:p.Met138Ile | |
| ENST00000352410.8:c.414G>A | ENSP00000318318.6:p.Met138Ile | |
| ENST00000535694.5:c.264G>A | ENSP00000440447.1:p.Met88Ile | |
| ENST00000561470.5:c.*310G>A | ENSP00000454267.1:n.*310G>A | |
| ENST00000562606.5:c.354G>A | ENSP00000457020.1:p.Met118Ile | |
| ENST00000562800.5:c.255+1240G>A | ENSP00000457619.1:n.255+1240G>A | |
| ENST00000563422.5:c.414G>A | ENSP00000457885.1:p.Met138Ile | |
| ENST00000563786.5:c.354G>A | ENSP00000455241.1:p.Met118Ile | |
| ENST00000564003.5:c.264G>A | ENSP00000454312.1:p.Met88Ile | |
| ENST00000564633.5:c.354G>A | ENSP00000455383.1:p.Met118Ile | |
| ENST00000565576.5:c.414G>A | ENSP00000454619.1:p.Met138Ile | |
| ENST00000566377.5:c.414G>A | ENSP00000455405.1:p.Met138Ile | |
| ENST00000567116.5:n.445G>A | ||
| ENST00000567132.5:c.372G>A | ENSP00000455972.1:p.Met124Ile | |
| ENST00000567177.1:c.375G>A | ENSP00000457013.1:p.Met125Ile | |
| ENST00000567570.5:c.354G>A | ENSP00000455477.1:p.Met118Ile | |
| ENST00000568828.5:c.378G>A | ENSP00000455065.1:p.Met126Ile | |
| ENST00000568840.1:n.523G>A | ||
| ENST00000568907.5:c.324G>A | ENSP00000457494.1:p.Met108Ile | |
| ENST00000569233.5:c.471G>A | ENSP00000454622.1:p.Met157Ile | |
| ENST00000569931.5:c.354G>A | ENSP00000455161.1:p.Met118Ile | |
| NM_001289155.1:c.414G>A | NP_001276084.1:p.Met138Ile | |
| NM_001289156.1:c.264G>A | NP_001276085.1:p.Met88Ile | |
| NM_001289157.1:c.414G>A | NP_001276086.1:p.Met138Ile | |
| NM_002435.2:c.414G>A | NP_002426.1:p.Met138Ile | |
| XM_011521592.1:c.402G>A | XP_011519894.1:p.Met134Ile | |
| XM_011521593.1:c.354G>A | XP_011519895.1:p.Met118Ile | |
| NM_001330372.1:c.354G>A | NP_001317301.1:p.Met118Ile | |
| XM_017022208.1:c.354G>A | XP_016877697.1:p.Met118Ile | |
| XM_017022209.2:c.264G>A | XP_016877698.1:p.Met88Ile | |
| NM_002435.3:c.414G>A MANE Select | NP_002426.1:p.Met138Ile | |
| NM_001289155.2:c.414G>A | NP_001276084.1:p.Met138Ile | |
| NM_001289156.2:c.264G>A | NP_001276085.1:p.Met88Ile | |
| NM_001289157.2:c.414G>A | NP_001276086.1:p.Met138Ile | |
| NM_001330372.2:c.354G>A | NP_001317301.1:p.Met118Ile |