Canonical Allele Identifier: CA433675970
Gene: ACTL11P HGNC NCBI

Linked Data

dbSNP Id: rs2082116151
gnomAD v3: 3-49873733-C-A
gnomAD v4: 3-49873733-C-A
MyVariant Identifiers: chr3:g.49911166C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49873733C>A , CM000665.2:g.49873733C>A GRCh38
NC_000003.11:g.49911166C>A , CM000665.1:g.49911166C>A GRCh37
NC_000003.10:g.49886170C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423971.2:n.3573G>T
ENST00000423971.1:n.4248G>T
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