Canonical Allele Identifier: CA220340421
Gene: THEM7P HGNC NCBI

Linked Data

dbSNP Id: rs76775909
gnomAD v2: 11-32364318-G-A
gnomAD v3: 11-32342772-G-A
gnomAD v4: 11-32342772-G-A
MyVariant Identifiers: chr11:g.32364318G>A (hg19) chr11:g.32342772G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32342772G>A , CM000673.2:g.32342772G>A GRCh38
NC_000011.9:g.32364318G>A , CM000673.1:g.32364318G>A GRCh37
NC_000011.8:g.32320894G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000525689.2:n.122+516C>T
ENST00000525689.1:n.122+516C>T
Search 100 bp 5'
Search 100 bp 3'