Linked Data
dbSNP Id:
rs1321188172
gnomAD v3:
14-105766144-C-T
gnomAD v4:
14-105766144-C-T
MyVariant Identifiers:
chr14:g.105766144C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.105766144C>T , CM000676.2:g.105766144C>T | GRCh38 |
| NC_000014.8:g.106232481C>T , CM000676.1:g.106232481C>T | GRCh37 |
| NC_000014.7:g.105303526C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641136.1:c.1257-147G>A |