Linked Data
ClinVar Variation Id:
1561675
ClinVar RCV Id:
RCV002212000
dbSNP Id:
rs1657158609
gnomAD v3:
1-197101157-G-A
gnomAD v4:
1-197101157-G-A
MyVariant Identifiers:
chr1:g.197070287G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197101157G>A , CM000663.2:g.197101157G>A | GRCh38 |
| NC_000001.10:g.197070287G>A , CM000663.1:g.197070287G>A | GRCh37 |
| NC_000001.9:g.195336910G>A | NCBI36 |
| NG_015867.1:g.50538C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367408.6:n.2108-4993C>T | ||
| ENST00000367409.9:c.8094C>T MANE Select | ENSP00000356379.4:p.Phe2698= | |
| ENST00000680265.1:c.8094C>T | ENSP00000505384.1:p.Phe2698= | |
| ENST00000680710.1:c.8094C>T | ENSP00000506676.1:p.Phe2698= | |
| ENST00000294732.11:c.4066-4993C>T | ENSP00000294732.7:n.4066-4993C>T | |
| ENST00000367408.5:c.1816-4993C>T | ENSP00000356378.1:n.1816-4993C>T | |
| ENST00000367409.8:c.8094C>T | ENSP00000356379.4:p.Phe2698= | |
| ENST00000612785.1:c.2052C>T | ENSP00000479244.1:p.Phe684= | |
| NM_001206846.1:c.4066-4993C>T | NP_001193775.1:n.4066-4993C>T | |
| NM_018136.4:c.8094C>T | NP_060606.3:p.Phe2698= | |
| NM_018136.5:c.8094C>T MANE Select | NP_060606.3:p.Phe2698= | |
| NM_001206846.2:c.4066-4993C>T | NP_001193775.1:n.4066-4993C>T |