Canonical Allele Identifier: CA2524765361
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1875455T>C , CM000682.2:g.1875455T>C GRCh38
NC_000020.10:g.1856101T>C , CM000682.1:g.1856101T>C GRCh37
NC_000020.9:g.1804101T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754467.1:n.433-7362A>G