Linked Data
dbSNP Id:
rs1657356931
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173903696C>G , CM000663.2:g.173903696C>G | GRCh38 |
| NC_000001.10:g.173872834C>G , CM000663.1:g.173872834C>G | GRCh37 |
| NC_000001.9:g.172139457C>G | NCBI36 |
| NG_012462.1:g.18683G>C , LRG_577:g.18683G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001365052.1:c.*193G>C | NP_001351981.1:n.*193G>C |