Canonical Allele Identifier: CA2695549885
Gene:

Linked Data

dbSNP Id: rs1219816086

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523690C>T , CM000663.2:g.34523690C>T GRCh38
NC_000001.10:g.34989291C>T , CM000663.1:g.34989291C>T GRCh37
NC_000001.9:g.34761878C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23889G>A
XR_001737964.1:n.991+23889G>A