Canonical Allele Identifier: CA1318169420
Gene:

Linked Data

dbSNP Id: rs1688119167

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006974C>T , CM000664.2:g.195006974C>T GRCh38
NC_000002.11:g.195871698C>T , CM000664.1:g.195871698C>T GRCh37
NC_000002.10:g.195579943C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52461G>A