Linked Data
MyVariant Identifiers:
chr5:g.37874329T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37874227T>C , CM000667.2:g.37874227T>C | GRCh38 |
| NC_000005.9:g.37874329T>C , CM000667.1:g.37874329T>C | GRCh37 |
| NC_000005.8:g.37910086T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001278094.1:c.-696T>C | NP_001265023.1:n.-696T>C | |
| NR_103441.1:n.371T>C | ||
| NR_103442.1:n.2680T>C | ||
| XM_011513926.1:c.-696T>C | XP_011512228.1:n.-696T>C | |
| NR_103441.2:n.371T>C | ||
| NR_145476.1:n.390T>C |