Linked Data
ClinVar Variation Id:
133757
ClinVar RCV Id:
RCV000120401
RCV000213879
RCV000468023
RCV000656815
RCV000662595
RCV003144130
RCV003149827
RCV003315737
dbSNP Id:
rs4988356
ExAC:
17:59763298 A / C
gnomAD v2:
17-59763298-A-C
gnomAD v3:
17-61685937-A-C
gnomAD v4:
17-61685937-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61685937A>C , CM000679.2:g.61685937A>C | GRCh38 |
| NC_000017.10:g.59763298A>C , CM000679.1:g.59763298A>C | GRCh37 |
| NC_000017.9:g.57118080A>C | NCBI36 |
| NG_007409.2:g.182623T>G , LRG_300:g.182623T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682066.1:c.2934T>G | ENSP00000507191.1:n.2934T>G | |
| ENST00000682073.1:n.1544T>G | ||
| ENST00000682433.1:n.1883T>G | ||
| ENST00000682453.1:c.2804T>G | ENSP00000506943.1:p.Val935Gly | |
| ENST00000682477.1:c.*2230T>G | ENSP00000507075.1:n.*2230T>G | |
| ENST00000682589.1:n.8681T>G | ||
| ENST00000682755.1:c.2582T>G | ENSP00000507660.1:p.Val861Gly | |
| ENST00000682989.1:c.2610-1797T>G | ENSP00000507786.1:n.2610-1797T>G | |
| ENST00000683039.1:c.2804T>G | ENSP00000508303.1:p.Val935Gly | |
| ENST00000683235.1:c.*219T>G | ENSP00000507646.1:n.*219T>G | |
| ENST00000683535.1:n.934T>G | ||
| ENST00000684471.1:n.1217T>G | ||
| ENST00000684584.1:c.2069-1797T>G | ENSP00000508044.1:n.2069-1797T>G | |
| ENST00000684626.1:n.1050T>G | ||
| ENST00000684769.1:c.994T>G | ENSP00000507691.1:n.994T>G | |
| ENST00000259008.7:c.2804T>G MANE Select | ENSP00000259008.2:p.Val935Gly | |
| ENST00000259008.6:c.2804T>G | ENSP00000259008.2:p.Val935Gly | |
| ENST00000577598.5:c.2804T>G | ENSP00000464654.1:p.Val935Gly | |
| NM_032043.2:c.2804T>G , LRG_300t1:c.2804T>G | NP_114432.2:p.Val935Gly | |
| XM_011525332.1:c.2864T>G | XP_011523634.1:p.Val955Gly | |
| XM_011525333.1:c.2864T>G | XP_011523635.1:p.Val955Gly | |
| XM_011525334.1:c.2864T>G | XP_011523636.1:p.Val955Gly | |
| XM_011525335.1:c.2804T>G | XP_011523637.1:p.Val935Gly | |
| XM_011525336.1:c.2744T>G | XP_011523638.1:p.Val915Gly | |
| XM_011525337.1:c.2663T>G | XP_011523639.1:p.Val888Gly | |
| XM_011525338.1:c.2381T>G | XP_011523640.1:p.Val794Gly | |
| XM_011525332.3:c.2864T>G | XP_011523634.1:p.Val955Gly | |
| XM_011525333.3:c.2864T>G | XP_011523635.1:p.Val955Gly | |
| XM_011525334.2:c.2864T>G | XP_011523636.1:p.Val955Gly | |
| XM_011525335.3:c.2804T>G | XP_011523637.1:p.Val935Gly | |
| XM_011525336.2:c.2744T>G | XP_011523638.1:p.Val915Gly | |
| XM_011525337.2:c.2663T>G | XP_011523639.1:p.Val888Gly | |
| XM_011525338.2:c.2381T>G | XP_011523640.1:p.Val794Gly | |
| XM_017025200.1:c.2321T>G | XP_016880689.1:p.Val774Gly | |
| XM_017025201.1:c.2321T>G | XP_016880690.1:p.Val774Gly | |
| XM_017025202.1:c.950T>G | XP_016880691.1:p.Val317Gly | |
| XM_017025203.1:c.950T>G | XP_016880692.1:p.Val317Gly | |
| NM_032043.3:c.2804T>G MANE Select | NP_114432.2:p.Val935Gly |