Linked Data
dbSNP Id:
rs1392781860
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186085601T>C , CM000666.2:g.186085601T>C | GRCh38 |
| NC_000004.11:g.187006755T>C , CM000666.1:g.187006755T>C | GRCh37 |
| NC_000004.10:g.187243749T>C | NCBI36 |
| NG_007278.1:g.21447T>C , LRG_117:g.21447T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698352.1:c.*2995T>C | ENSP00000513675.1:n.*2995T>C | |
| ENST00000698353.1:n.3318T>C | ||
| ENST00000698354.1:c.*728T>C | ENSP00000513676.1:n.*728T>C | |
| ENST00000296795.8:c.*728T>C MANE Select | ENSP00000296795.3:n.*728T>C | |
| ENST00000296795.7:c.*728T>C | ENSP00000296795.2:n.*728T>C | |
| NM_003265.3:c.*728T>C MANE Select | NP_003256.1:n.*728T>C |