Linked Data
MyVariant Identifiers:
chr5:g.156541884G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157114873G>T , CM000667.2:g.157114873G>T | GRCh38 |
| NC_000005.9:g.156541884G>T , CM000667.1:g.156541884G>T | GRCh37 |
| NC_000005.8:g.156474462G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524219.2:c.-293-7911C>A | ENSP00000430328.2:n.-293-7911C>A | |
| ENST00000524219.1:c.-293-7911C>A | ENSP00000430328.1:n.-293-7911C>A |