Linked Data
ClinVar Variation Id:
136582
ClinVar RCV Id:
RCV000124032
RCV000212296
RCV000411186
RCV000410111
RCV000588076
RCV001086934
RCV001798416
RCV003315841
dbSNP Id:
rs45566938
ExAC:
17:59938865 C / A
gnomAD v2:
17-59938865-C-A
gnomAD v3:
17-61861504-C-A
gnomAD v4:
17-61861504-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61861504C>A , CM000679.2:g.61861504C>A | GRCh38 |
| NC_000017.10:g.59938865C>A , CM000679.1:g.59938865C>A | GRCh37 |
| NC_000017.9:g.57293647C>A | NCBI36 |
| NG_007409.2:g.7056G>T , LRG_300:g.7056G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000577913.2:c.36G>T | ENSP00000462274.2:p.Gly12= | |
| ENST00000584322.2:c.36G>T | ENSP00000463272.2:p.Gly12= | |
| ENST00000682369.1:c.36G>T | ENSP00000507450.1:p.Gly12= | |
| ENST00000682453.1:c.36G>T | ENSP00000506943.1:p.Gly12= | |
| ENST00000682477.1:c.36G>T | ENSP00000507075.1:p.Gly12= | |
| ENST00000682589.1:n.1777G>T | ||
| ENST00000682755.1:c.36G>T | ENSP00000507660.1:p.Gly12= | |
| ENST00000682989.1:c.36G>T | ENSP00000507786.1:p.Gly12= | |
| ENST00000683039.1:c.36G>T | ENSP00000508303.1:p.Gly12= | |
| ENST00000683235.1:c.36G>T | ENSP00000507646.1:p.Gly12= | |
| ENST00000683381.1:c.36G>T | ENSP00000508184.1:p.Gly12= | |
| ENST00000683672.1:c.-93+1780G>T | ENSP00000506781.1:n.-93+1780G>T | |
| ENST00000259008.7:c.36G>T MANE Select | ENSP00000259008.2:p.Gly12= | |
| ENST00000259008.6:c.36G>T | ENSP00000259008.2:p.Gly12= | |
| ENST00000577598.5:c.36G>T | ENSP00000464654.1:p.Gly12= | |
| ENST00000577913.1:c.36G>T | ENSP00000462274.1:p.Gly12= | |
| NM_032043.2:c.36G>T , LRG_300t1:c.36G>T | NP_114432.2:p.Gly12= | |
| XM_011525332.1:c.36G>T | XP_011523634.1:p.Gly12= | |
| XM_011525333.1:c.36G>T | XP_011523635.1:p.Gly12= | |
| XM_011525334.1:c.36G>T | XP_011523636.1:p.Gly12= | |
| XM_011525335.1:c.36G>T | XP_011523637.1:p.Gly12= | |
| XM_011525336.1:c.36G>T | XP_011523638.1:p.Gly12= | |
| XM_011525337.1:c.36G>T | XP_011523639.1:p.Gly12= | |
| XM_011525339.1:c.36G>T | XP_011523641.1:p.Gly12= | |
| XM_011525340.1:c.36G>T | XP_011523642.1:p.Gly12= | |
| XM_011525341.1:c.36G>T | XP_011523643.1:p.Gly12= | |
| XM_011525332.3:c.36G>T | XP_011523634.1:p.Gly12= | |
| XM_011525333.3:c.36G>T | XP_011523635.1:p.Gly12= | |
| XM_011525334.2:c.36G>T | XP_011523636.1:p.Gly12= | |
| XM_011525335.3:c.36G>T | XP_011523637.1:p.Gly12= | |
| XM_011525336.2:c.36G>T | XP_011523638.1:p.Gly12= | |
| XM_011525337.2:c.36G>T | XP_011523639.1:p.Gly12= | |
| XM_011525339.3:c.36G>T | XP_011523641.1:p.Gly12= | |
| XM_011525340.3:c.36G>T | XP_011523642.1:p.Gly12= | |
| XM_011525341.3:c.36G>T | XP_011523643.1:p.Gly12= | |
| NM_032043.3:c.36G>T MANE Select | NP_114432.2:p.Gly12= |