Linked Data
gnomAD v4:
5-71719692-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719692G>C , CM000667.2:g.71719692G>C | GRCh38 |
| NC_000005.9:g.71015519G>C , CM000667.1:g.71015519G>C | GRCh37 |
| NC_000005.8:g.71051275G>C | NCBI36 |
| NG_015988.1:g.5530G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.160-188G>C MANE Select | ENSP00000296777.4:n.160-188G>C | |
| ENST00000296777.4:c.160-188G>C | ENSP00000296777.4:n.160-188G>C | |
| ENST00000513096.1:n.114G>C | ||
| NM_004291.3:c.160-188G>C | NP_004282.1:n.160-188G>C | |
| NM_004291.4:c.160-188G>C MANE Select | NP_004282.1:n.160-188G>C |