Linked Data
dbSNP Id:
rs1208285
gnomAD v4:
6-133837662-T-A
MyVariant Identifiers:
chr6:g.134158800T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.133837662T>A , CM000668.2:g.133837662T>A | GRCh38 |
| NC_000006.11:g.134158800T>A , CM000668.1:g.134158800T>A | GRCh37 |
| NC_000006.10:g.134200493T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_027030.1:n.659T>A (LINC01312) | ||
| NR_109982.1:n.478+8215A>T (TARID) |