Canonical Allele Identifier: CA1912720779
Gene:

Linked Data

dbSNP Id: rs1589010426

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812631A>C , CM000672.2:g.57812631A>C GRCh38
NC_000010.10:g.59572391A>C , CM000672.1:g.59572391A>C GRCh37
NC_000010.9:g.59242397A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34661T>G
XR_001747454.1:n.85+34661T>G