Linked Data
MyVariant Identifiers:
chr8:g.24814236G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956722G>T , CM000670.2:g.24956722G>T | GRCh38 |
| NC_000008.10:g.24814236G>T , CM000670.1:g.24814236G>T | GRCh37 |
| NC_000008.9:g.24870153G>T | NCBI36 |
| NG_008492.1:g.4896C>A , LRG_259:g.4896C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.1:c.-207C>A | ENSP00000482169.1:n.-207C>A | |
| NM_006158.4:c.-207C>A , LRG_259t1:c.-207C>A | NP_006149.2:n.-207C>A |