Linked Data
dbSNP Id:
rs1743761159
gnomAD v3:
4-39446917-A-C
gnomAD v4:
4-39446917-A-C
MyVariant Identifiers:
chr4:g.39448537A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.39446917A>C , CM000666.2:g.39446917A>C | GRCh38 |
| NC_000004.11:g.39448537A>C , CM000666.1:g.39448537A>C | GRCh37 |
| NC_000004.10:g.39124932A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257408.5:c.2191A>C MANE Select | ENSP00000257408.4:p.Arg731= | |
| ENST00000257408.4:c.2191A>C | ENSP00000257408.4:p.Arg731= | |
| NM_175737.3:c.2191A>C | NP_783864.1:p.Arg731= | |
| XM_005262644.1:c.2164A>C | XP_005262701.1:p.Arg722= | |
| NM_175737.4:c.2191A>C MANE Select | NP_783864.1:p.Arg731= |