Linked Data
dbSNP Id:
rs1806130486
gnomAD v4:
8-54628148-T-C
MyVariant Identifiers:
chr8:g.55540708T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.54628148T>C , CM000670.2:g.54628148T>C | GRCh38 |
| NC_000008.10:g.55540708T>C , CM000670.1:g.55540708T>C | GRCh37 |
| NC_000008.9:g.55703261T>C | NCBI36 |
| NG_009840.1:g.17082T>C | |
| NG_009840.2:g.17082T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220676.2:c.4266T>C MANE Select | ENSP00000220676.1:p.Asn1422= | |
| ENST00000636932.1:c.787+5860T>C | ENSP00000489857.1:n.787+5860T>C | |
| ENST00000637698.1:c.787+5860T>C | ENSP00000490104.1:n.787+5860T>C | |
| ENST00000220676.1:c.4266T>C | ENSP00000220676.1:p.Asn1422= | |
| NM_006269.1:c.4266T>C | NP_006260.1:p.Asn1422= | |
| XM_017013721.1:c.4287T>C | XP_016869210.1:p.Asn1429= | |
| XM_017013722.1:c.4266T>C | XP_016869211.1:p.Asn1422= | |
| NM_001375654.1:c.787+5860T>C | NP_001362583.1:n.787+5860T>C | |
| NM_006269.2:c.4266T>C MANE Select | NP_006260.1:p.Asn1422= |