Linked Data
dbSNP Id:
rs1489664649
gnomAD v4:
12-6974207-T-C
MyVariant Identifiers:
chr12:g.6974207T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6974207T>C , CM000674.2:g.6974207T>C | GRCh38 |
| NC_000012.11:g.7083369T>C , CM000674.1:g.7083369T>C | GRCh37 |
| NC_000012.10:g.6953630T>C | NCBI36 |
| NG_021408.1:g.8427T>C | |
| NG_021408.2:g.8427T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599672.6:c.169-132T>C MANE Select | ENSP00000470560.1:n.169-132T>C | |
| ENST00000261406.7:c.151-132T>C | ENSP00000476966.2:n.151-132T>C | |
| ENST00000539196.2:c.32-132T>C | ||
| ENST00000599672.5:c.169-132T>C | ENSP00000470560.1:n.169-132T>C | |
| ENST00000607161.5:c.172-132T>C | ENSP00000480420.1:n.172-132T>C | |
| ENST00000611981.1:n.180-132T>C | ||
| ENST00000620255.1:n.158-132T>C | ||
| NM_006331.7:c.169-132T>C | NP_006322.4:n.169-132T>C | |
| XM_011520907.1:c.169-132T>C | XP_011519209.1:n.169-132T>C | |
| NM_001320049.1:c.169-132T>C | NP_001306978.1:n.169-132T>C | |
| NR_135131.1:n.312-132T>C | ||
| NM_006331.8:c.169-132T>C MANE Select | NP_006322.4:n.169-132T>C | |
| NM_001320049.2:c.169-132T>C | NP_001306978.1:n.169-132T>C | |
| NR_135131.2:n.180-132T>C |