Linked Data
gnomAD v4:
16-67939978-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67939978T>C , CM000678.2:g.67939978T>C | GRCh38 |
| NC_000016.9:g.67973881T>C , CM000678.1:g.67973881T>C | GRCh37 |
| NC_000016.8:g.66531382T>C | NCBI36 |
| NG_009778.1:g.9135A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.1249A>G MANE Select | ENSP00000264005.5:p.Ile417Val | |
| ENST00000264005.9:c.1249A>G | ENSP00000264005.5:p.Ile417Val | |
| ENST00000570369.5:c.252A>G | ||
| ENST00000573538.5:c.987A>G | ENSP00000463220.1:n.987A>G | |
| NM_000229.1:c.1249A>G | NP_000220.1:p.Ile417Val | |
| NM_000229.2:c.1249A>G MANE Select | NP_000220.1:p.Ile417Val |