Linked Data
dbSNP Id:
rs778499185
ExAC:
12:6132872 C / T
gnomAD v2:
12-6132872-C-T
gnomAD v3:
12-6023706-C-T
gnomAD v4:
12-6023706-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6023706C>T , CM000674.2:g.6023706C>T | GRCh38 |
| NC_000012.11:g.6132872C>T , CM000674.1:g.6132872C>T | GRCh37 |
| NC_000012.10:g.6003133C>T | NCBI36 |
| NG_009072.1:g.105965G>A | |
| NG_009072.2:g.105965G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.3304G>A MANE Select | ENSP00000261405.5:p.Asp1102Asn | |
| ENST00000261405.9:c.3304G>A | ENSP00000261405.5:p.Asp1102Asn | |
| ENST00000538635.5:n.421-29772G>A | ||
| NM_000552.3:c.3304G>A | NP_000543.2:p.Asp1102Asn | |
| NM_000552.4:c.3304G>A | NP_000543.2:p.Asp1102Asn | |
| NM_000552.5:c.3304G>A MANE Select | NP_000543.3:p.Asp1102Asn |