Canonical Allele Identifier: CA337618387
Gene:

Linked Data

dbSNP Id: rs34761704

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8372684C>T , CM000686.2:g.8372684C>T GRCh38
NC_000024.9:g.8240725C>T , CM000686.1:g.8240725C>T GRCh37
NC_000024.8:g.8300725C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000452458.1:n.444C>T