Canonical Allele Identifier: CA2684112978
Gene: ACTL6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100646916del , CM000669.2:g.100646916del GRCh38
NC_000007.13:g.100244539del , CM000669.1:g.100244539del GRCh37
NC_000007.12:g.100082475del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000160382.10:c.936+58del MANE Select ENSP00000160382.5:n.936+58del
ENST00000160382.9:c.936+58del ENSP00000160382.5:n.936+58del
ENST00000487125.1:n.498+58del
NM_016188.4:c.936+58del NP_057272.1:n.936+58del
XR_927476.1:n.1043+58del
NR_134539.1:n.1043+58del
NM_016188.5:c.936+58del MANE Select NP_057272.1:n.936+58del
NR_134539.2:n.1030+58del