Linked Data
dbSNP Id:
rs554699410
gnomAD v4:
8-24956705-C-T
MyVariant Identifiers:
chr8:g.24814219C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956705C>T , CM000670.2:g.24956705C>T | GRCh38 |
| NC_000008.10:g.24814219C>T , CM000670.1:g.24814219C>T | GRCh37 |
| NC_000008.9:g.24870136C>T | NCBI36 |
| NG_008492.1:g.4913G>A , LRG_259:g.4913G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.1:c.-190G>A | ENSP00000482169.1:n.-190G>A | |
| ENST00000615973.1:n.17G>A | ||
| NM_006158.4:c.-190G>A , LRG_259t1:c.-190G>A | NP_006149.2:n.-190G>A |