Linked Data
dbSNP Id:
rs1187931904
gnomAD v3:
11-14076981-T-C
gnomAD v4:
11-14076981-T-C
MyVariant Identifiers:
chr11:g.14076981T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14076981T>C , CM000673.2:g.14076981T>C | GRCh38 |
| NC_000011.9:g.14098528T>C , CM000673.1:g.14098528T>C | GRCh37 |
| NC_000011.8:g.14055104T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000576479.4:c.553+1563T>C MANE Select | ENSP00000460236.1:n.553+1563T>C | |
| ENST00000576479.3:c.553+1563T>C | ENSP00000460236.1:n.553+1563T>C | |
| NM_006108.3:c.553+1563T>C | NP_006099.2:n.553+1563T>C | |
| NM_006108.4:c.553+1563T>C MANE Select | NP_006099.2:n.553+1563T>C |