Canonical Allele Identifier: CA1898741271
Gene:

Linked Data

dbSNP Id: rs1835464063

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075709C>T , CM000672.2:g.29075709C>T GRCh38
NC_000010.10:g.29364638C>T , CM000672.1:g.29364638C>T GRCh37
NC_000010.9:g.29404644C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3783C>T