Linked Data
ClinVar Variation Id:
374135
ClinVar RCV Id:
RCV000487533
RCV000415245
RCV000690328
RCV001128279
RCV001128278
RCV001128280
RCV001198358
RCV003993948
dbSNP Id:
rs370966353
ExAC:
19:38964366 C / T
gnomAD v2:
19-38964366-C-T
gnomAD v3:
19-38473726-C-T
gnomAD v4:
19-38473726-C-T
MyVariant Identifiers:
chr19:g.38964366C>T (hg19)
chr19:g.38964366_38964369delinsTGGA (hg19)
chr19:g.38473726C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38473726C>T , CM000681.2:g.38473726C>T | GRCh38 |
| NC_000019.9:g.38964366C>T , CM000681.1:g.38964366C>T | GRCh37 |
| NC_000019.8:g.43656206C>T | NCBI36 |
| NG_008866.1:g.45027C>T , LRG_766:g.45027C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.4115C>T | ENSP00000471601.2:p.Ala1372Val | |
| ENST00000359596.8:c.4115C>T MANE Select | ENSP00000352608.2:p.Ala1372Val | |
| ENST00000355481.8:c.4115C>T | ENSP00000347667.3:p.Ala1372Val | |
| ENST00000359596.7:c.4115C>T | ENSP00000352608.2:p.Ala1372Val | |
| ENST00000360985.7:c.4112C>T | ENSP00000354254.4:p.Ala1371Val | |
| NM_000540.2:c.4115C>T , LRG_766t1:c.4115C>T | NP_000531.2:p.Ala1372Val | |
| NM_001042723.1:c.4115C>T | NP_001036188.1:p.Ala1372Val | |
| XM_006723317.1:c.4115C>T | XP_006723380.1:p.Ala1372Val | |
| XM_006723319.1:c.4115C>T | XP_006723382.1:p.Ala1372Val | |
| XM_011527204.1:c.4112C>T | XP_011525506.1:p.Ala1371Val | |
| XM_011527205.1:c.4115C>T | XP_011525507.1:p.Ala1372Val | |
| XM_006723317.2:c.4115C>T | XP_006723380.1:p.Ala1372Val | |
| XM_006723319.2:c.4115C>T | XP_006723382.1:p.Ala1372Val | |
| XM_011527205.2:c.4115C>T | XP_011525507.1:p.Ala1372Val | |
| XR_001753735.1:n.4198C>T | ||
| NM_000540.3:c.4115C>T MANE Select | NP_000531.2:p.Ala1372Val | |
| NM_001042723.2:c.4115C>T | NP_001036188.1:p.Ala1372Val |