Linked Data
MyVariant Identifiers:
chr5:g.156541908T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157114897T>G , CM000667.2:g.157114897T>G | GRCh38 |
| NC_000005.9:g.156541908T>G , CM000667.1:g.156541908T>G | GRCh37 |
| NC_000005.8:g.156474486T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524219.2:c.-293-7935A>C | ENSP00000430328.2:n.-293-7935A>C | |
| ENST00000524219.1:c.-293-7935A>C | ENSP00000430328.1:n.-293-7935A>C |