Canonical Allele Identifier: CA299344144
Gene:

Linked Data

dbSNP Id: rs911707905
MyVariant Identifiers: chr18:g.39057839T>C (hg19) chr18:g.41477875T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477875T>C , CM000680.2:g.41477875T>C GRCh38
NC_000018.9:g.39057839T>C , CM000680.1:g.39057839T>C GRCh37
NC_000018.8:g.37311837T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26259T>C
Search 100 bp 5'
Search 100 bp 3'