Linked Data
dbSNP Id:
rs1845997040
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444478C>G , CM000673.2:g.2444478C>G | GRCh38 |
| NC_000011.9:g.2465708C>G , CM000673.1:g.2465708C>G | GRCh37 |
| NC_000011.8:g.2422284C>G | NCBI36 |
| NG_008935.1:g.4488C>G , LRG_287:g.4488C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696290.1:c.-1733G>C MANE Select | ENSP00000512529.1:n.-1733G>C | |
| XR_930984.1:n.93G>C | ||
| NM_014555.4:c.-1733G>C MANE Select | NP_055370.1:n.-1733G>C |