Canonical Allele Identifier: CA2504001951
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007198C>T , CM000664.2:g.195007198C>T GRCh38
NC_000002.11:g.195871922C>T , CM000664.1:g.195871922C>T GRCh37
NC_000002.10:g.195580167C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52237G>A