Linked Data
MyVariant Identifiers:
chr12:g.58159942G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766159G>C , CM000674.2:g.57766159G>C | GRCh38 |
| NC_000012.11:g.58159942G>C , CM000674.1:g.58159942G>C | GRCh37 |
| NC_000012.10:g.56446209G>C | NCBI36 |
| NG_007076.1:g.6035C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.146C>G | ||
| ENST00000713544.1:c.234C>G | ENSP00000518840.1:p.Ala78= | |
| ENST00000713545.1:c.234C>G | ENSP00000518841.1:p.Ala78= | |
| ENST00000228606.9:c.234C>G MANE Select | ENSP00000228606.4:p.Ala78= | |
| ENST00000228606.8:c.234C>G | ENSP00000228606.4:p.Ala78= | |
| ENST00000546496.1:n.62C>G | ||
| ENST00000546609.1:c.146C>G | ||
| ENST00000547344.5:n.288C>G | ||
| ENST00000552186.1:n.353C>G | ||
| NM_000785.3:c.234C>G | NP_000776.1:p.Ala78= | |
| NM_000785.4:c.234C>G MANE Select | NP_000776.1:p.Ala78= |