Linked Data
gnomAD v4:
5-71719677-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719677C>A , CM000667.2:g.71719677C>A | GRCh38 |
| NC_000005.9:g.71015504C>A , CM000667.1:g.71015504C>A | GRCh37 |
| NC_000005.8:g.71051260C>A | NCBI36 |
| NG_015988.1:g.5515C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.160-203C>A MANE Select | ENSP00000296777.4:n.160-203C>A | |
| ENST00000296777.4:c.160-203C>A | ENSP00000296777.4:n.160-203C>A | |
| ENST00000513096.1:n.99C>A | ||
| NM_004291.3:c.160-203C>A | NP_004282.1:n.160-203C>A | |
| NM_004291.4:c.160-203C>A MANE Select | NP_004282.1:n.160-203C>A |