Linked Data
gnomAD v4:
14-74493496-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493496C>T , CM000676.2:g.74493496C>T | GRCh38 |
| NC_000014.8:g.74960199C>T , CM000676.1:g.74960199C>T | GRCh37 |
| NC_000014.7:g.74029952C>T | NCBI36 |
| NG_007117.1:g.4886G>A | |
| NG_033074.1:g.4777C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-64+74G>A | ENSP00000450887.1:n.-64+74G>A | |
| ENST00000555619.5:c.-222G>A | ENSP00000451112.1:n.-222G>A | |
| ENST00000556009.5:c.147+535G>A | ||
| NM_001363688.1:c.-222G>A | NP_001350617.1:n.-222G>A | |
| NM_006432.4:c.-222G>A | NP_006423.1:n.-222G>A |