Canonical Allele Identifier: CA1161925208
Gene:

Linked Data

dbSNP Id: rs1639363375

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523559T>C , CM000663.2:g.34523559T>C GRCh38
NC_000001.10:g.34989160T>C , CM000663.1:g.34989160T>C GRCh37
NC_000001.9:g.34761747T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+24020A>G
XR_001737964.1:n.991+24020A>G