Linked Data
dbSNP Id:
rs1935101493
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564923A>G , CM000684.2:g.36564923A>G | GRCh38 |
| NC_000022.10:g.36960970A>G , CM000684.1:g.36960970A>G | GRCh37 |
| NC_000022.9:g.35290916A>G | NCBI36 |
| NG_031861.1:g.142721T>C | |
| NG_031861.2:g.142936T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.437-37T>C MANE Select | ENSP00000300105.6:n.437-37T>C | |
| ENST00000300105.6:c.437-37T>C | ENSP00000300105.6:n.437-37T>C | |
| NM_006078.3:c.437-37T>C | NP_006069.1:n.437-37T>C | |
| NM_006078.4:c.437-37T>C | NP_006069.1:n.437-37T>C | |
| XM_017028531.2:c.179-37T>C | XP_016884020.1:n.179-37T>C | |
| NM_001379051.1:c.368-37T>C | NP_001365980.1:n.368-37T>C | |
| NM_006078.5:c.437-37T>C MANE Select | NP_006069.1:n.437-37T>C | |
| NR_166440.1:n.1803-37T>C |