Linked Data
dbSNP Id:
rs938303546
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150851801A>C , CM000669.2:g.150851801A>C | GRCh38 |
| NC_000007.13:g.150548889A>C , CM000669.1:g.150548889A>C | GRCh37 |
| NC_000007.12:g.150179822A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000467291.5:c.-92-314A>C | ENSP00000418328.1:n.-92-314A>C | |
| ENST00000493429.5:c.-92-314A>C | ENSP00000418614.1:n.-92-314A>C | |
| XM_011516008.1:c.-181-314A>C | XP_011514310.1:n.-181-314A>C | |
| XM_011516009.1:c.-92-314A>C | XP_011514311.1:n.-92-314A>C | |
| XR_928169.1:n.296-10356T>G | ||
| XR_928170.1:n.426-10356T>G | ||
| XR_928171.1:n.298-10356T>G | ||
| XM_017011944.1:c.-92-314A>C | XP_016867433.1:n.-92-314A>C | |
| XM_017011945.1:c.-92-314A>C | XP_016867434.1:n.-92-314A>C | |
| XR_928169.2:n.302-10356T>G | ||
| XR_928171.2:n.302-10356T>G |