Linked Data
dbSNP Id:
rs928770495
gnomAD v4:
7-155463322-C-A
MyVariant Identifiers:
chr7:g.155463322C>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155463322C>A , CM000669.2:g.155463322C>A | GRCh38 |
| NC_000007.13:g.155256017C>A , CM000669.1:g.155256017C>A | GRCh37 |
| NC_000007.12:g.154948778C>A | NCBI36 |
| NG_007124.1:g.11603C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297375.4:c.*635C>A MANE Select | ENSP00000297375.4:n.*635C>A | |
| NM_001427.3:c.*635C>A | NP_001418.2:n.*635C>A | |
| NM_001427.4:c.*635C>A MANE Select | NP_001418.2:n.*635C>A |