Canonical Allele Identifier: CA15532005
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.110407907C>T , CM000669.2:g.110407907C>T GRCh38
NC_000007.13:g.110047964C>T , CM000669.1:g.110047964C>T GRCh37
NC_000007.12:g.109835200C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744982.1:n.604+24904G>A
XR_927863.2:n.367+24904G>A