Linked Data
ClinVar Variation Id:
329097
dbSNP Id:
rs779541890
ExAC:
19:39013656 C / T
gnomAD v2:
19-39013656-C-T
gnomAD v3:
19-38523016-C-T
gnomAD v4:
19-38523016-C-T
MyVariant Identifiers:
chr19:g.39013656C>T (hg19)
chr19:g.39013656_39013661delinsTGCTGA (hg19)
chr19:g.38523016C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38523016C>T , CM000681.2:g.38523016C>T | GRCh38 |
| NC_000019.9:g.39013656C>T , CM000681.1:g.39013656C>T | GRCh37 |
| NC_000019.8:g.43705496C>T | NCBI36 |
| NG_008866.1:g.94317C>T , LRG_766:g.94317C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.10199-12C>T | ENSP00000471601.2:n.10199-12C>T | |
| ENST00000359596.8:c.10260-12C>T MANE Select | ENSP00000352608.2:n.10260-12C>T | |
| ENST00000355481.8:c.10260-12C>T | ENSP00000347667.3:n.10260-12C>T | |
| ENST00000359596.7:c.10260-12C>T | ENSP00000352608.2:n.10260-12C>T | |
| ENST00000360985.7:c.10257-12C>T | ENSP00000354254.4:n.10257-12C>T | |
| ENST00000594335.5:c.3662-12C>T | ||
| ENST00000599547.5:c.1067-12C>T | ||
| NM_000540.2:c.10260-12C>T , LRG_766t1:c.10260-12C>T | NP_000531.2:n.10260-12C>T | |
| NM_001042723.1:c.10260-12C>T | NP_001036188.1:n.10260-12C>T | |
| XM_006723317.1:c.10260-12C>T | XP_006723380.1:n.10260-12C>T | |
| XM_006723319.1:c.10260-12C>T | XP_006723382.1:n.10260-12C>T | |
| XM_011527204.1:c.10257-12C>T | XP_011525506.1:n.10257-12C>T | |
| XM_011527205.1:c.10260-12C>T | XP_011525507.1:n.10260-12C>T | |
| XM_006723317.2:c.10260-12C>T | XP_006723380.1:n.10260-12C>T | |
| XM_006723319.2:c.10260-12C>T | XP_006723382.1:n.10260-12C>T | |
| XM_011527205.2:c.10260-12C>T | XP_011525507.1:n.10260-12C>T | |
| NM_000540.3:c.10260-12C>T MANE Select | NP_000531.2:n.10260-12C>T | |
| NM_001042723.2:c.10260-12C>T | NP_001036188.1:n.10260-12C>T |