Linked Data
MyVariant Identifiers:
chr2:g.27308068A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27085200A>T , CM000664.2:g.27085200A>T | GRCh38 |
| NC_000002.11:g.27308068A>T , CM000664.1:g.27308068A>T | GRCh37 |
| NC_000002.10:g.27161572A>T | NCBI36 |
| NG_012199.1:g.3458A>T | |
| NG_046849.1:g.11634A>T | |
| NG_012199.2:g.3458A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380320.9:c.2616A>T MANE Select | ENSP00000369677.4:p.Ala872= | |
| ENST00000380320.8:c.2616A>T | ENSP00000369677.4:p.Ala872= | |
| ENST00000433140.1:c.608A>T | ||
| NM_007046.3:c.2616A>T | NP_008977.1:p.Ala872= | |
| XM_006711928.2:c.2575+192A>T | XP_006711991.1:n.2575+192A>T | |
| NM_007046.4:c.2616A>T MANE Select | NP_008977.1:p.Ala872= |