Linked Data
ClinVar Variation Id:
1593997
dbSNP Id:
rs376180682
ExAC:
19:39076775 G / A
gnomAD v2:
19-39076775-G-A
gnomAD v3:
19-38586135-G-A
gnomAD v4:
19-38586135-G-A
COSMIC:
COSM1393429
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38586135G>A , CM000681.2:g.38586135G>A | GRCh38 |
| NC_000019.9:g.39076775G>A , CM000681.1:g.39076775G>A | GRCh37 |
| NC_000019.8:g.43768615G>A | NCBI36 |
| NG_008866.1:g.157436G>A , LRG_766:g.157436G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1849G>A | ||
| ENST00000688602.1:c.3246G>A | ||
| ENST00000689936.1:c.3218G>A | ||
| ENST00000692547.1:n.306G>A | ||
| ENST00000359596.8:c.14913G>A MANE Select | ENSP00000352608.2:p.Thr4971= | |
| ENST00000355481.8:c.14898G>A | ENSP00000347667.3:p.Thr4966= | |
| ENST00000359596.7:c.14913G>A | ENSP00000352608.2:p.Thr4971= | |
| ENST00000360985.7:c.14895G>A | ENSP00000354254.4:p.Thr4965= | |
| NM_000540.2:c.14913G>A , LRG_766t1:c.14913G>A | NP_000531.2:p.Thr4971= | |
| NM_001042723.1:c.14898G>A | NP_001036188.1:p.Thr4966= | |
| XM_006723317.1:c.14895G>A | XP_006723380.1:p.Thr4965= | |
| XM_006723319.1:c.14880G>A | XP_006723382.1:p.Thr4960= | |
| XM_011527204.1:c.14910G>A | XP_011525506.1:p.Thr4970= | |
| XM_011527205.1:c.14826G>A | XP_011525507.1:p.Thr4942= | |
| XM_006723317.2:c.14895G>A | XP_006723380.1:p.Thr4965= | |
| XM_006723319.2:c.14880G>A | XP_006723382.1:p.Thr4960= | |
| XM_011527205.2:c.14826G>A | XP_011525507.1:p.Thr4942= | |
| NM_000540.3:c.14913G>A MANE Select | NP_000531.2:p.Thr4971= | |
| NM_001042723.2:c.14898G>A | NP_001036188.1:p.Thr4966= |