Linked Data
dbSNP Id:
rs782174861
gnomAD v2:
12-6979336-G-T
gnomAD v4:
12-6870172-G-T
MyVariant Identifiers:
chr12:g.6979336G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6870172G>T , CM000674.2:g.6870172G>T | GRCh38 |
| NC_000012.11:g.6979336G>T , CM000674.1:g.6979336G>T | GRCh37 |
| NC_000012.10:g.6849597G>T | NCBI36 |
| NG_011948.1:g.7753G>T | |
| NG_013308.1:g.8186C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396705.10:c.631+36G>T MANE Select | ENSP00000379933.4:n.631+36G>T | |
| ENST00000229270.8:c.742+36G>T | ENSP00000229270.4:n.742+36G>T | |
| ENST00000396705.9:c.631+36G>T | ENSP00000379933.4:n.631+36G>T | |
| ENST00000474253.1:n.120+36G>T | ||
| ENST00000488464.6:c.385+36G>T | ENSP00000475620.1:n.385+36G>T | |
| ENST00000535434.5:c.385+36G>T | ENSP00000443599.1:n.385+36G>T | |
| ENST00000613953.4:c.742+36G>T | ENSP00000484435.1:n.742+36G>T | |
| NM_000365.5:c.631+36G>T | NP_000356.1:n.631+36G>T | |
| NM_001159287.1:c.742+36G>T | NP_001152759.1:n.742+36G>T | |
| NM_001258026.1:c.385+36G>T | NP_001244955.1:n.385+36G>T | |
| XR_002957378.1:n.1639+36G>T | ||
| NM_000365.6:c.631+36G>T MANE Select | NP_000356.1:n.631+36G>T | |
| NM_001258026.2:c.385+36G>T | NP_001244955.1:n.385+36G>T |