Canonical Allele Identifier: CA1818149800
Gene:

Linked Data

dbSNP Id: rs1814939104

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999709G>C , CM000670.2:g.126999709G>C GRCh38
NC_000008.10:g.128011954G>C , CM000670.1:g.128011954G>C GRCh37
NC_000008.9:g.128081136G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-6846G>C