Canonical Allele Identifier: CA74565707
Gene: ACTL11P HGNC NCBI

Linked Data

dbSNP Id: rs1053498607
gnomAD v4: 3-49873732-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49873732A>G , CM000665.2:g.49873732A>G GRCh38
NC_000003.11:g.49911165A>G , CM000665.1:g.49911165A>G GRCh37
NC_000003.10:g.49886169A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423971.2:n.3574T>C
ENST00000423971.1:n.4249T>C