Canonical Allele Identifier: CA2529707721
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006930G>T , CM000664.2:g.195006930G>T GRCh38
NC_000002.11:g.195871654G>T , CM000664.1:g.195871654G>T GRCh37
NC_000002.10:g.195579899G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52505C>A