Linked Data
dbSNP Id:
rs1565476692
gnomAD v2:
12-7945248-G-C
gnomAD v3:
12-7792652-G-C
gnomAD v4:
12-7792652-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7792652G>C , CM000674.2:g.7792652G>C | GRCh38 |
| NC_000012.11:g.7945248G>C , CM000674.1:g.7945248G>C | GRCh37 |
| NC_000012.10:g.7836515G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229307.9:c.152-298G>C MANE Select | ENSP00000229307.4:n.152-298G>C | |
| ENST00000229307.8:c.152-298G>C | ENSP00000229307.4:n.152-298G>C | |
| ENST00000526286.1:c.152-298G>C | ENSP00000435288.1:n.152-298G>C | |
| ENST00000526434.2:n.334-336G>C | ||
| ENST00000541267.5:c.80-298G>C | ENSP00000444434.1:n.80-298G>C | |
| NM_001297698.1:c.152-298G>C | NP_001284627.1:n.152-298G>C | |
| NM_024865.3:c.152-298G>C | NP_079141.2:n.152-298G>C | |
| XM_011520850.1:c.152-298G>C | XP_011519152.1:n.152-298G>C | |
| XM_011520851.1:c.80-298G>C | XP_011519153.1:n.80-298G>C | |
| XM_011520852.1:c.-183-336G>C | XP_011519154.1:n.-183-336G>C | |
| NM_024865.4:c.152-298G>C MANE Select | NP_079141.2:n.152-298G>C | |
| NM_001297698.2:c.152-298G>C | NP_001284627.1:n.152-298G>C |