Canonical Allele Identifier: CA433675946
Gene: ACTL11P HGNC NCBI

Linked Data

gnomAD v4: 3-49873725-T-C
MyVariant Identifiers: chr3:g.49911158T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49873725T>C , CM000665.2:g.49873725T>C GRCh38
NC_000003.11:g.49911158T>C , CM000665.1:g.49911158T>C GRCh37
NC_000003.10:g.49886162T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423971.2:n.3581A>G
ENST00000423971.1:n.4256A>G
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