Linked Data
MyVariant Identifiers:
chr12:g.72388285A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71994505A>T , CM000674.2:g.71994505A>T | GRCh38 |
| NC_000012.11:g.72388285A>T , CM000674.1:g.72388285A>T | GRCh37 |
| NC_000012.10:g.70674552A>T | NCBI36 |
| NG_008279.1:g.60660A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000333850.4:c.1008A>T MANE Select | ENSP00000329093.3:p.Ser336= | |
| ENST00000333850.3:c.1008A>T | ENSP00000329093.3:p.Ser336= | |
| NM_173353.3:c.1008A>T | NP_775489.2:p.Ser336= | |
| XM_011537899.1:c.414A>T | XP_011536201.1:p.Ser138= | |
| NM_173353.4:c.1008A>T MANE Select | NP_775489.2:p.Ser336= |