Canonical Allele Identifier: CA433675973
Gene: ACTL11P HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.49911166C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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