Canonical Allele Identifier:
CA1313350138
Community Standard Title: NC_000002.12:g.184597742A=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.184597742A= , CM000664.2:g.184597742A= | GRCh38 |
| NC_000002.11:g.185462469A= , CM000664.1:g.185462469A= | GRCh37 |
| NC_000002.10:g.185170714A= | NCBI36 |
| NG_046950.1:g.4377A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_171621.1:n.655+526T= | |
| XM_011512285.1:c.618+526T= | XP_011510587.1:n.618+526T= |
| XR_923658.1:n.518T= | |
| XR_923659.1:n.518T= | |
| XR_923660.1:n.519T= |