Linked Data
MyVariant Identifiers:
chr16:g.67974317G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940414G>C , CM000678.2:g.67940414G>C | GRCh38 |
| NC_000016.9:g.67974317G>C , CM000678.1:g.67974317G>C | GRCh37 |
| NC_000016.8:g.66531818G>C | NCBI36 |
| NG_009778.1:g.8699C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.813C>G MANE Select | ENSP00000264005.5:p.Thr271= | |
| ENST00000264005.9:c.813C>G | ENSP00000264005.5:p.Thr271= | |
| ENST00000570369.5:c.156-340C>G | ||
| ENST00000570980.1:c.597C>G | ENSP00000464651.1:p.Thr199= | |
| ENST00000573538.5:c.551C>G | ENSP00000463220.1:n.551C>G | |
| NM_000229.1:c.813C>G | NP_000220.1:p.Thr271= | |
| NM_000229.2:c.813C>G MANE Select | NP_000220.1:p.Thr271= |