Linked Data
MyVariant Identifiers:
chr12:g.21327578A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174644A>C , CM000674.2:g.21174644A>C | GRCh38 |
| NC_000012.11:g.21327578A>C , CM000674.1:g.21327578A>C | GRCh37 |
| NC_000012.10:g.21218845A>C | NCBI36 |
| NG_011745.1:g.48451A>C , LRG_1022:g.48451A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.294A>C MANE Select | ENSP00000256958.2:p.Gly98= | |
| ENST00000256958.2:c.294A>C | ENSP00000256958.2:p.Gly98= | |
| ENST00000543498.5:c.426-2132A>C | ||
| NM_006446.4:c.294A>C , LRG_1022t1:c.294A>C | NP_006437.3:p.Gly98= | |
| NM_006446.5:c.294A>C MANE Select | NP_006437.3:p.Gly98= |