Linked Data
dbSNP Id:
rs1788364178
gnomAD v3:
6-160437036-C-A
gnomAD v4:
6-160437036-C-A
MyVariant Identifiers:
chr6:g.160858068C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160437036C>A , CM000668.2:g.160437036C>A | GRCh38 |
| NC_000006.11:g.160858068C>A , CM000668.1:g.160858068C>A | GRCh37 |
| NC_000006.10:g.160778058C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000275300.3:c.1113C>A MANE Select | ENSP00000275300.2:p.Arg371= | |
| ENST00000275300.2:c.1113C>A | ENSP00000275300.2:p.Arg371= | |
| NM_021977.3:c.1113C>A | NP_068812.1:p.Arg371= | |
| XM_005267106.3:c.720C>A | XP_005267163.1:p.Arg240= | |
| XM_011536075.1:c.657C>A | XP_011534377.1:p.Arg219= | |
| XM_011536076.1:c.657C>A | XP_011534378.1:p.Arg219= | |
| XM_011536077.1:c.657C>A | XP_011534379.1:p.Arg219= | |
| XR_245546.1:n.1018-5725C>A | ||
| XM_005267106.5:c.720C>A | XP_005267163.1:p.Arg240= | |
| XM_011536075.2:c.657C>A | XP_011534377.1:p.Arg219= | |
| XM_011536076.3:c.657C>A | XP_011534378.1:p.Arg219= | |
| XM_017011203.2:c.657C>A | XP_016866692.1:p.Arg219= | |
| XR_001743588.1:n.1057C>A | ||
| XR_001743589.1:n.1018-5725C>A | ||
| NM_021977.4:c.1113C>A MANE Select | NP_068812.1:p.Arg371= |