Canonical Allele Identifier: CA15465886
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131125651C>G , CM000668.2:g.131125651C>G GRCh38
NC_000006.11:g.131446791C>G , CM000668.1:g.131446791C>G GRCh37
NC_000006.10:g.131488484C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428022.2:n.95+4086G>C
XR_942994.1:n.95+4086G>C
XR_001744341.1:n.472+4138G>C
XR_428022.3:n.524+4086G>C
XR_942994.2:n.524+4086G>C