Canonical Allele Identifier: CA576714443
Gene: ACTL6B HGNC NCBI

Linked Data

dbSNP Id: rs774118514
gnomAD v2: 7-100244571-C-T
gnomAD v4: 7-100646948-C-T
MyVariant Identifiers: chr7:g.100244571C>T (hg19) chr7:g.100646948C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100646948C>T , CM000669.2:g.100646948C>T GRCh38
NC_000007.13:g.100244571C>T , CM000669.1:g.100244571C>T GRCh37
NC_000007.12:g.100082507C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000160382.10:c.936+23G>A MANE Select ENSP00000160382.5:n.936+23G>A
ENST00000160382.9:c.936+23G>A ENSP00000160382.5:n.936+23G>A
ENST00000487125.1:n.498+23G>A
NM_016188.4:c.936+23G>A NP_057272.1:n.936+23G>A
XR_927476.1:n.1043+23G>A
NR_134539.1:n.1043+23G>A
NM_016188.5:c.936+23G>A MANE Select NP_057272.1:n.936+23G>A
NR_134539.2:n.1030+23G>A
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