Canonical Allele Identifier:
CA1487775130
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.116928293G>C , CM000666.2:g.116928293G>C | GRCh38 |
| NC_000004.11:g.117849449G>C , CM000666.1:g.117849449G>C | GRCh37 |
| NC_000004.10:g.118068897G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741796.1:n.668+28C>G | ||
| XR_001741797.1:n.619+28C>G | ||
| XR_001741798.1:n.671+28C>G | ||
| XR_001741800.1:n.671+28C>G |