Linked Data
ClinVar Variation Id:
384894
dbSNP Id:
rs376726966
ExAC:
17:63554604 G / A
gnomAD v2:
17-63554604-G-A
gnomAD v3:
17-65558486-G-A
gnomAD v4:
17-65558486-G-A
COSMIC:
COSM3937511
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.65558486G>A , CM000679.2:g.65558486G>A | GRCh38 |
| NC_000017.10:g.63554604G>A , CM000679.1:g.63554604G>A | GRCh37 |
| NC_000017.9:g.60985066G>A | NCBI36 |
| NG_012142.1:g.8137C>T , LRG_296:g.8137C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307078.10:c.135C>T MANE Select | ENSP00000302625.5:p.Val45= | |
| ENST00000307078.9:c.135C>T | ENSP00000302625.5:p.Val45= | |
| ENST00000375702.5:c.135C>T | ENSP00000364854.5:p.Val45= | |
| ENST00000544103.2:c.135C>T | ENSP00000441151.2:p.Val45= | |
| ENST00000577278.1:c.135C>T | ENSP00000464264.1:p.Val45= | |
| ENST00000577662.1:c.450C>T | ||
| ENST00000580513.1:c.135C>T | ENSP00000463761.1:p.Val45= | |
| ENST00000585045.1:c.135C>T | ENSP00000463192.1:p.Val45= | |
| ENST00000611991.1:c.135C>T | ENSP00000481191.1:p.Val45= | |
| ENST00000618960.4:c.135C>T | ENSP00000478916.1:p.Val45= | |
| NM_004655.3:c.135C>T , LRG_296t1:c.135C>T | NP_004646.3:p.Val45= | |
| XM_011525319.1:c.135C>T | XP_011523621.1:p.Val45= | |
| XM_011525320.1:c.135C>T | XP_011523622.1:p.Val45= | |
| XM_011525321.1:c.135C>T | XP_011523623.1:p.Val45= | |
| XM_011525322.1:c.135C>T | XP_011523624.1:p.Val45= | |
| NM_001363813.1:c.135C>T | NP_001350742.1:p.Val45= | |
| NM_004655.4:c.135C>T MANE Select | NP_004646.3:p.Val45= | |
| XM_011525319.2:c.135C>T | XP_011523621.1:p.Val45= | |
| XM_011525321.2:c.135C>T | XP_011523623.1:p.Val45= | |
| XM_017025192.1:c.135C>T | XP_016880681.1:p.Val45= | |
| XM_017025193.1:c.135C>T | XP_016880682.1:p.Val45= |