Linked Data
MyVariant Identifiers:
chr5:g.37874326A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37874224A>T , CM000667.2:g.37874224A>T | GRCh38 |
| NC_000005.9:g.37874326A>T , CM000667.1:g.37874326A>T | GRCh37 |
| NC_000005.8:g.37910083A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NM_001278094.1:c.-699A>T | NP_001265023.1:n.-699A>T | |
| NR_103441.1:n.368A>T | ||
| NR_103442.1:n.2677A>T | ||
| XM_011513926.1:c.-699A>T | XP_011512228.1:n.-699A>T | |
| NR_103441.2:n.368A>T | ||
| NR_145476.1:n.387A>T |