MyVariant.info:
GRCh37
chr21:g.43443498C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.42023389C>G , CM000683.2:g.42023389C>G | GRCh38 |
| NC_000021.8:g.43443498C>G , CM000683.1:g.43443498C>G | GRCh37 |
| NC_000021.7:g.42316567C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027273.2:n.163-917C>G | ||
| NR_119384.1:n.392-917C>G | ||
| NR_119385.1:n.209-917C>G |