Linked Data
gnomAD v4:
4-153684229-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.153684229G>C , CM000666.2:g.153684229G>C | GRCh38 |
| NC_000004.11:g.154605381G>C , CM000666.1:g.154605381G>C | GRCh37 |
| NC_000004.10:g.154824831G>C | NCBI36 |
| NG_016229.1:g.4941G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646900.2:c.-279G>C | ENSP00000493968.2:n.-279G>C | |
| ENST00000646900.1:c.-279G>C | ENSP00000493968.1:n.-279G>C | |
| XM_017008573.1:c.-578G>C | XP_016864062.1:n.-578G>C |