Canonical Allele Identifier: CA1691656438
Gene:

Linked Data

dbSNP Id: rs1388079609

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957839C>T , CM000669.2:g.17957839C>T GRCh38
NC_000007.13:g.17997462C>T , CM000669.1:g.17997462C>T GRCh37
NC_000007.12:g.17963987C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927078.1:n.271-831C>T