Linked Data
ClinVar Variation Id:
1374848
ClinVar RCV Id:
RCV001879362
dbSNP Id:
rs769894290
ExAC:
14:75470235 G / A
gnomAD v2:
14-75470235-G-A
gnomAD v3:
14-75003532-G-A
gnomAD v4:
14-75003532-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75003532G>A , CM000676.2:g.75003532G>A | GRCh38 |
| NC_000014.8:g.75470235G>A , CM000676.1:g.75470235G>A | GRCh37 |
| NC_000014.7:g.74539988G>A | NCBI36 |
| NG_013333.1:g.5624G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.285-19G>A MANE Select | ENSP00000266126.5:n.285-19G>A | |
| ENST00000266126.9:c.285-19G>A | ENSP00000266126.5:n.285-19G>A | |
| ENST00000553401.5:c.258-19G>A | ENSP00000451681.1:n.258-19G>A | |
| ENST00000553539.1:n.561G>A | ||
| ENST00000555522.1:n.343-19G>A | ||
| ENST00000556028.5:c.285-19G>A | ENSP00000452311.1:n.285-19G>A | |
| NM_014239.3:c.285-19G>A | NP_055054.1:n.285-19G>A | |
| NM_014239.4:c.285-19G>A MANE Select | NP_055054.1:n.285-19G>A |