Canonical Allele Identifier: CA1619157145
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439993G= , CM000668.2:g.31439993G= GRCh38
NC_000006.11:g.31407770G= , CM000668.1:g.31407770G= GRCh37
NC_000006.10:g.31515749G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926694.1:n.114C=