Canonical Allele Identifier: CA368542916
Gene: ACTL6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.100244622T>A (hg19) chr7:g.100646999T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100646999T>A , CM000669.2:g.100646999T>A GRCh38
NC_000007.13:g.100244622T>A , CM000669.1:g.100244622T>A GRCh37
NC_000007.12:g.100082558T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000160382.10:c.908A>T MANE Select ENSP00000160382.5:p.Glu303Val
ENST00000160382.9:c.908A>T ENSP00000160382.5:p.Glu303Val
ENST00000487125.1:n.470A>T
NM_016188.4:c.908A>T NP_057272.1:p.Glu303Val
XR_927476.1:n.1015A>T
NR_134539.1:n.1015A>T
NM_016188.5:c.908A>T MANE Select NP_057272.1:p.Glu303Val
NR_134539.2:n.1002A>T
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