Canonical Allele Identifier: CA1728106729
Gene:

Linked Data

dbSNP Id: rs546871857

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388472C>T , CM000669.2:g.97388472C>T GRCh38
NC_000007.13:g.97017784C>T , CM000669.1:g.97017784C>T GRCh37
NC_000007.12:g.96855720C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59825G>A