Linked Data
dbSNP Id:
rs1578950658
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.153684220A>C , CM000666.2:g.153684220A>C | GRCh38 |
| NC_000004.11:g.154605372A>C , CM000666.1:g.154605372A>C | GRCh37 |
| NC_000004.10:g.154824822A>C | NCBI36 |
| NG_016229.1:g.4932A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646900.2:c.-288A>C | ENSP00000493968.2:n.-288A>C | |
| ENST00000646900.1:c.-288A>C | ENSP00000493968.1:n.-288A>C | |
| XM_017008573.1:c.-587A>C | XP_016864062.1:n.-587A>C |