Canonical Allele Identifier: CA1609069952
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525190C= , CM000668.2:g.8525190C= GRCh38
NC_000006.11:g.8525423C= , CM000668.1:g.8525423C= GRCh37
NC_000006.10:g.8470422C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038979.1:n.626-33395C=
NR_038980.1:n.649-33395C=