Linked Data
dbSNP Id:
rs1042701700
gnomAD v4:
1-17334107-A-C
MyVariant Identifiers:
chr1:g.17334107A>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17334107A>C , CM000663.2:g.17334107A>C | GRCh38 |
| NC_000001.10:g.17660602A>C , CM000663.1:g.17660602A>C | GRCh37 |
| NC_000001.9:g.17533189A>C | NCBI36 |
| NG_023261.2:g.30918A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.340+98A>C MANE Select | ENSP00000364597.4:n.340+98A>C | |
| ENST00000375453.5:c.340+98A>C | ENSP00000364602.1:n.340+98A>C | |
| NM_012387.2:c.340+98A>C | NP_036519.2:n.340+98A>C | |
| XM_011541150.1:c.340+98A>C | XP_011539452.1:n.340+98A>C | |
| XM_011541151.1:c.340+98A>C | XP_011539453.1:n.340+98A>C | |
| XM_011541152.1:c.-80+98A>C | XP_011539454.1:n.-80+98A>C | |
| XM_011541153.1:c.340+98A>C | XP_011539455.1:n.340+98A>C | |
| XM_011541154.1:c.340+98A>C | XP_011539456.1:n.340+98A>C | |
| XM_011541155.1:c.340+98A>C | XP_011539457.1:n.340+98A>C | |
| XM_011541156.1:c.340+98A>C | XP_011539458.1:n.340+98A>C | |
| XM_011541157.1:c.-373+98A>C | XP_011539459.1:n.-373+98A>C | |
| XM_011541154.2:c.340+98A>C | XP_011539456.1:n.340+98A>C | |
| NM_012387.3:c.340+98A>C MANE Select | NP_036519.2:n.340+98A>C |