Linked Data
dbSNP Id:
rs1562310420
gnomAD v4:
6-31463955-C-T
MyVariant Identifiers:
chr6:g.31431732C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31463955C>T , CM000668.2:g.31463955C>T | GRCh38 |
| NC_000006.11:g.31431732C>T , CM000668.1:g.31431732C>T | GRCh37 |
| NC_000006.10:g.31539711C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040662.1:n.685C>T |