Linked Data
dbSNP Id:
rs2145681813
gnomAD v4:
19-38517432-T-C
MyVariant Identifiers:
chr19:g.39008072T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38517432T>C , CM000681.2:g.38517432T>C | GRCh38 |
| NC_000019.9:g.39008072T>C , CM000681.1:g.39008072T>C | GRCh37 |
| NC_000019.8:g.43699912T>C | NCBI36 |
| NG_008866.1:g.88733T>C , LRG_766:g.88733T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.9698T>C | ENSP00000471601.2:n.9698T>C | |
| ENST00000359596.8:c.9759T>C MANE Select | ENSP00000352608.2:p.Ile3253= | |
| ENST00000355481.8:c.9759T>C | ENSP00000347667.3:p.Ile3253= | |
| ENST00000359596.7:c.9759T>C | ENSP00000352608.2:p.Ile3253= | |
| ENST00000360985.7:c.9756T>C | ENSP00000354254.4:p.Ile3252= | |
| ENST00000594335.5:c.3161T>C | ||
| ENST00000599547.5:c.566T>C | ||
| NM_000540.2:c.9759T>C , LRG_766t1:c.9759T>C | NP_000531.2:p.Ile3253= | |
| NM_001042723.1:c.9759T>C | NP_001036188.1:p.Ile3253= | |
| XM_006723317.1:c.9759T>C | XP_006723380.1:p.Ile3253= | |
| XM_006723319.1:c.9759T>C | XP_006723382.1:p.Ile3253= | |
| XM_011527204.1:c.9756T>C | XP_011525506.1:p.Ile3252= | |
| XM_011527205.1:c.9759T>C | XP_011525507.1:p.Ile3253= | |
| XM_006723317.2:c.9759T>C | XP_006723380.1:p.Ile3253= | |
| XM_006723319.2:c.9759T>C | XP_006723382.1:p.Ile3253= | |
| XM_011527205.2:c.9759T>C | XP_011525507.1:p.Ile3253= | |
| NM_000540.3:c.9759T>C MANE Select | NP_000531.2:p.Ile3253= | |
| NM_001042723.2:c.9759T>C | NP_001036188.1:p.Ile3253= |