Linked Data
gnomAD v4:
14-74493449-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493449T>C , CM000676.2:g.74493449T>C | GRCh38 |
| NC_000014.8:g.74960152T>C , CM000676.1:g.74960152T>C | GRCh37 |
| NC_000014.7:g.74029905T>C | NCBI36 |
| NG_007117.1:g.4933A>G | |
| NG_033074.1:g.4730T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-63-112A>G | ENSP00000450887.1:n.-63-112A>G | |
| ENST00000555619.5:c.-175A>G | ENSP00000451112.1:n.-175A>G | |
| ENST00000556009.5:c.147+582A>G | ||
| NM_001363688.1:c.-175A>G | NP_001350617.1:n.-175A>G | |
| NM_006432.4:c.-175A>G | NP_006423.1:n.-175A>G |