Canonical Allele Identifier:
CA12786828
Community Standard Title: NC_000008.11:g.23726713G>T
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23726713G>T , CM000670.2:g.23726713G>T | GRCh38 |
| NC_000008.10:g.23584226G>T , CM000670.1:g.23584226G>T | GRCh37 |
| NC_000008.9:g.23640171G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001745838.1:n.178C>A | |
| XR_001745839.1:n.154-102C>A | |
| XR_001745842.1:n.1312+57963G>T | |
| XR_247144.3:n.139-102C>A | |
| XR_247144.4:n.154-102C>A | |
| XR_949587.1:n.138-102C>A | |
| XR_949587.2:n.154-102C>A |