Canonical Allele Identifier: CA2817734438
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890401T>C , CM000683.2:g.32890401T>C GRCh38
NC_000021.8:g.34262709T>C , CM000683.1:g.34262709T>C GRCh37
NC_000021.7:g.33184579T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937669.1:n.460-3177T>C
XR_937669.2:n.1038-3177T>C