Linked Data
dbSNP Id:
rs1480723512
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108439880A>T , CM000685.2:g.108439880A>T | GRCh38 |
| NC_000023.10:g.107683110A>T , CM000685.1:g.107683110A>T | GRCh37 |
| NC_000023.9:g.107569766A>T | NCBI36 |
| NG_011977.1:g.4957A>T | |
| NG_012059.2:g.4595T>A | |
| NG_011977.2:g.4957A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.-246A>T MANE Select | ENSP00000331902.7:n.-246A>T | |
| ENST00000477429.1:n.37A>T | ||
| NM_000495.4:c.-246A>T | NP_000486.1:n.-246A>T | |
| NM_033380.2:c.-246A>T | NP_203699.1:n.-246A>T | |
| XM_005262070.2:c.-246A>T | XP_005262127.1:n.-246A>T | |
| XM_005262072.3:c.-246A>T | XP_005262129.1:n.-246A>T | |
| XM_006724616.2:c.-121+85A>T | XP_006724679.1:n.-121+85A>T | |
| XM_011530850.1:c.-246A>T | XP_011529152.1:n.-246A>T | |
| NM_000495.5:c.-246A>T | NP_000486.1:n.-246A>T | |
| NM_033380.3:c.-246A>T MANE Select | NP_203699.1:n.-246A>T |