Linked Data
MyVariant Identifiers:
chr2:g.61605503T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.61378368T>C , CM000664.2:g.61378368T>C | GRCh38 |
| NC_000002.11:g.61605503T>C , CM000664.1:g.61605503T>C | GRCh37 |
| NC_000002.10:g.61459007T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398571.7:c.1071A>G MANE Select | ENSP00000381577.2:p.Thr357= | |
| ENST00000398571.6:c.1071A>G | ENSP00000381577.2:p.Thr357= | |
| ENST00000453133.1:c.597A>G | ||
| NM_014709.3:c.1071A>G | NP_055524.3:p.Thr357= | |
| NM_014709.4:c.1071A>G MANE Select | NP_055524.3:p.Thr357= |