Linked Data
dbSNP Id:
rs1785693414
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32177609T>A , CM000668.2:g.32177609T>A | GRCh38 |
| NC_000006.11:g.32145386T>A , CM000668.1:g.32145386T>A | GRCh37 |
| NC_000006.10:g.32253364T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336984.6:c.-10+392A>T | ENSP00000337463.6:n.-10+392A>T | |
| ENST00000395497.5:c.-75A>T | ENSP00000378875.1:n.-75A>T | |
| NM_032741.4:c.-10+392A>T | NP_116130.2:n.-10+392A>T | |
| XM_011514234.1:c.-75A>T | XP_011512536.1:n.-75A>T | |
| XM_005248806.2:c.-385A>T | XP_005248863.1:n.-385A>T | |
| NM_032741.5:c.-10+392A>T | NP_116130.2:n.-10+392A>T |