Linked Data
dbSNP Id:
rs1210162779
gnomAD v2:
14-74960046-G-C
gnomAD v3:
14-74493343-G-C
gnomAD v4:
14-74493343-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493343G>C , CM000676.2:g.74493343G>C | GRCh38 |
| NC_000014.8:g.74960046G>C , CM000676.1:g.74960046G>C | GRCh37 |
| NC_000014.7:g.74029799G>C | NCBI36 |
| NG_007117.1:g.5039C>G | |
| NG_033074.1:g.4624G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-63-6C>G | ENSP00000450887.1:n.-63-6C>G | |
| ENST00000555619.5:c.-69C>G | ENSP00000451112.1:n.-69C>G | |
| ENST00000556009.5:c.147+688C>G | ||
| ENST00000557510.5:c.-69C>G | ENSP00000451206.1:n.-69C>G | |
| NM_006432.3:c.-69C>G | NP_006423.1:n.-69C>G | |
| NM_001363688.1:c.-69C>G | NP_001350617.1:n.-69C>G | |
| NM_006432.4:c.-69C>G | NP_006423.1:n.-69C>G |