Linked Data
dbSNP Id:
rs1555132569
gnomAD v2:
12-6979424-C-T
gnomAD v4:
12-6870260-C-T
MyVariant Identifiers:
chr12:g.6979424C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6870260C>T , CM000674.2:g.6870260C>T | GRCh38 |
| NC_000012.11:g.6979424C>T , CM000674.1:g.6979424C>T | GRCh37 |
| NC_000012.10:g.6849685C>T | NCBI36 |
| NG_011948.1:g.7841C>T | |
| NG_013308.1:g.8098G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396705.10:c.632-5C>T MANE Select | ENSP00000379933.4:n.632-5C>T | |
| ENST00000229270.8:c.743-5C>T | ENSP00000229270.4:n.743-5C>T | |
| ENST00000396705.9:c.632-5C>T | ENSP00000379933.4:n.632-5C>T | |
| ENST00000474253.1:n.121-5C>T | ||
| ENST00000488464.6:c.386-5C>T | ENSP00000475620.1:n.386-5C>T | |
| ENST00000535434.5:c.386-5C>T | ENSP00000443599.1:n.386-5C>T | |
| ENST00000613953.4:c.743-5C>T | ENSP00000484435.1:n.743-5C>T | |
| NM_000365.5:c.632-5C>T | NP_000356.1:n.632-5C>T | |
| NM_001159287.1:c.743-5C>T | NP_001152759.1:n.743-5C>T | |
| NM_001258026.1:c.386-5C>T | NP_001244955.1:n.386-5C>T | |
| XR_002957378.1:n.1640-5C>T | ||
| NM_000365.6:c.632-5C>T MANE Select | NP_000356.1:n.632-5C>T | |
| NM_001258026.2:c.386-5C>T | NP_001244955.1:n.386-5C>T |