Canonical Allele Identifier: CA1912720812
Gene:

Linked Data

dbSNP Id: rs766062795
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812691C>A , CM000672.2:g.57812691C>A GRCh38
NC_000010.10:g.59572451C>A , CM000672.1:g.59572451C>A GRCh37
NC_000010.9:g.59242457C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34601G>T
XR_001747454.1:n.85+34601G>T
Search 100 bp 5'
Search 100 bp 3'