Canonical Allele Identifier: CA1111626473
Gene:

Linked Data

dbSNP Id: rs1355202087
gnomAD v3: 8-20734899-A-C
gnomAD v4: 8-20734899-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734899A>C , CM000670.2:g.20734899A>C GRCh38
NC_000008.10:g.20592410A>C , CM000670.1:g.20592410A>C GRCh37
NC_000008.9:g.20636690A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55547A>C
Search 100 bp 5'
Search 100 bp 3'