Linked Data
ClinVar Variation Id:
663264
dbSNP Id:
rs376746368
ExAC:
15:75182912 A / G
gnomAD v2:
15-75182912-A-G
gnomAD v3:
15-74890571-A-G
gnomAD v4:
15-74890571-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74890571A>G , CM000677.2:g.74890571A>G | GRCh38 |
| NC_000015.9:g.75182912A>G , CM000677.1:g.75182912A>G | GRCh37 |
| NC_000015.8:g.72969965A>G | NCBI36 |
| NG_008921.1:g.5503A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352410.9:c.61A>G MANE Select | ENSP00000318318.6:p.Met21Val | |
| ENST00000323744.10:c.61A>G | ENSP00000318192.6:p.Met21Val | |
| ENST00000352410.8:c.61A>G | ENSP00000318318.6:p.Met21Val | |
| ENST00000535694.5:c.-7+482A>G | ENSP00000440447.1:n.-7+482A>G | |
| ENST00000561470.5:c.173A>G | ENSP00000454267.1:p.Asp58Gly | |
| ENST00000562606.5:c.1A>G | ENSP00000457020.1:p.Met1Val | |
| ENST00000562800.5:c.61A>G | ENSP00000457619.1:p.Met21Val | |
| ENST00000563422.5:c.61A>G | ENSP00000457885.1:p.Met21Val | |
| ENST00000563786.5:c.1A>G | ENSP00000455241.1:p.Met1Val | |
| ENST00000564003.5:c.-7+482A>G | ENSP00000454312.1:n.-7+482A>G | |
| ENST00000564633.5:c.1A>G | ENSP00000455383.1:p.Met1Val | |
| ENST00000565576.5:c.61A>G | ENSP00000454619.1:p.Met21Val | |
| ENST00000566377.5:c.61A>G | ENSP00000455405.1:p.Met21Val | |
| ENST00000567116.5:n.92A>G | ||
| ENST00000567132.5:c.61A>G | ENSP00000455972.1:p.Met21Val | |
| ENST00000567177.1:c.22A>G | ENSP00000457013.1:p.Met8Val | |
| ENST00000567570.5:c.1A>G | ENSP00000455477.1:p.Met1Val | |
| ENST00000568303.1:n.178A>G | ||
| ENST00000568828.5:c.61A>G | ENSP00000455065.1:p.Met21Val | |
| ENST00000568840.1:n.170A>G | ||
| ENST00000568907.5:c.61A>G | ENSP00000457494.1:p.Met21Val | |
| ENST00000569233.5:c.61A>G | ENSP00000454622.1:p.Met21Val | |
| ENST00000569931.5:c.1A>G | ENSP00000455161.1:p.Met1Val | |
| NM_001289155.1:c.61A>G | NP_001276084.1:p.Met21Val | |
| NM_001289156.1:c.-7+482A>G | NP_001276085.1:n.-7+482A>G | |
| NM_001289157.1:c.61A>G | NP_001276086.1:p.Met21Val | |
| NM_002435.2:c.61A>G | NP_002426.1:p.Met21Val | |
| XM_011521592.1:c.49A>G | XP_011519894.1:p.Met17Val | |
| XM_011521593.1:c.1A>G | XP_011519895.1:p.Met1Val | |
| NM_001330372.1:c.1A>G | NP_001317301.1:p.Met1Val | |
| XM_017022208.1:c.1A>G | XP_016877697.1:p.Met1Val | |
| XM_017022209.2:c.-7+482A>G | XP_016877698.1:n.-7+482A>G | |
| NM_002435.3:c.61A>G MANE Select | NP_002426.1:p.Met21Val | |
| NM_001289155.2:c.61A>G | NP_001276084.1:p.Met21Val | |
| NM_001289156.2:c.-7+482A>G | NP_001276085.1:n.-7+482A>G | |
| NM_001289157.2:c.61A>G | NP_001276086.1:p.Met21Val | |
| NM_001330372.2:c.1A>G | NP_001317301.1:p.Met1Val |