Canonical Allele Identifier: CA2490662411
Gene:

Linked Data

dbSNP Id: rs1239017039

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.14925988C>T , CM000664.2:g.14925988C>T GRCh38
NC_000002.11:g.15066112C>T , CM000664.1:g.15066112C>T GRCh37
NC_000002.10:g.14983563C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922818.1:n.205-146841G>A