Canonical Allele Identifier: CA1912720768
Gene:

Linked Data

dbSNP Id: rs1589010411
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812602C>A , CM000672.2:g.57812602C>A GRCh38
NC_000010.10:g.59572362C>A , CM000672.1:g.59572362C>A GRCh37
NC_000010.9:g.59242368C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34690G>T
XR_001747454.1:n.85+34690G>T
Search 100 bp 5'
Search 100 bp 3'