dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122454839C>A , CM000672.2:g.122454839C>A | GRCh38 |
| NC_000010.10:g.124214355C>A , CM000672.1:g.124214355C>A | GRCh37 |
| NC_000010.9:g.124204345C>A | NCBI36 |
| NG_011725.1:g.5177C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000528446.1:c.112C>A MANE Select | ENSP00000436682.1:p.Arg38= | |
| NM_001099667.1:c.112C>A | NP_001093137.1:p.Arg38= | |
| XR_946382.1:n.1827+3656G>T | ||
| XR_946383.1:n.1827+3656G>T | ||
| XR_946384.1:n.1576+3656G>T | ||
| NM_001099667.2:c.112C>A | NP_001093137.1:p.Arg38= | |
| XR_946382.2:n.1855+3656G>T | ||
| XR_946383.2:n.1855+3656G>T | ||
| XR_946384.2:n.1580+3656G>T | ||
| NM_001099667.3:c.112C>A MANE Select | NP_001093137.1:p.Arg38= |