Canonical Allele Identifier: CA1161925272
Gene:

Linked Data

dbSNP Id: rs1639364812

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523682C>G , CM000663.2:g.34523682C>G GRCh38
NC_000001.10:g.34989283C>G , CM000663.1:g.34989283C>G GRCh37
NC_000001.9:g.34761870C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947171.1:n.1073+23897G>C
XR_001737964.1:n.991+23897G>C