Linked Data
dbSNP Id:
rs1725101714
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.121697058A>G , CM000666.2:g.121697058A>G | GRCh38 |
| NC_000004.11:g.122618213A>G , CM000666.1:g.122618213A>G | GRCh37 |
| NC_000004.10:g.122837663A>G | NCBI36 |
| NG_032042.1:g.4935T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296511.9:c.-231T>C | ENSP00000296511.5:n.-231T>C |