Canonical Allele Identifier: CA2721793254
Gene:

Linked Data

dbSNP Id: rs2132200962

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812899C>A , CM000672.2:g.57812899C>A GRCh38
NC_000010.10:g.59572659C>A , CM000672.1:g.59572659C>A GRCh37
NC_000010.9:g.59242665C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34393G>T
XR_001747454.1:n.85+34393G>T