Linked Data
MyVariant Identifiers:
chr13:g.33628122A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33053985A>C , CM000675.2:g.33053985A>C | GRCh38 |
| NC_000013.10:g.33628122A>C , CM000675.1:g.33628122A>C | GRCh37 |
| NC_000013.9:g.32526122A>C | NCBI36 |
| NG_011485.1:g.42552A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.1038A>C MANE Select | ENSP00000369442.3:p.Ser346= | |
| ENST00000380099.3:c.1038A>C | ENSP00000369442.3:p.Ser346= | |
| ENST00000487852.1:n.1046A>C | ||
| NM_004795.3:c.1038A>C | NP_004786.2:p.Ser346= | |
| XM_006719895.1:c.117A>C | XP_006719958.1:p.Ser39= | |
| XM_006719895.2:c.117A>C | XP_006719958.1:p.Ser39= | |
| NM_004795.4:c.1038A>C MANE Select | NP_004786.2:p.Ser346= |