Canonical Allele Identifier: CA4387155

Gene: ACTL6B

Linked Data

• dbSNP Id: rs369078607
• ExAC: 7:100244928 G / T
• gnomAD v2: 7-100244928-G-T
• gnomAD v3: 7-100647305-G-T
• gnomAD v4: 7-100647305-G-T
• MyVariant Identifiers: chr7:g.100244928G>T (hg19) ; chr7:g.100647305G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100647305G>T , CM000669.2:g.100647305G>T	GRCh38
NC_000007.13:g.100244928G>T , CM000669.1:g.100244928G>T	GRCh37
NC_000007.12:g.100082864G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000160382.10:c.760-21C>A MANE Select	ENSP00000160382.5:n.760-21C>A
ENST00000160382.9:c.760-21C>A	ENSP00000160382.5:n.760-21C>A
ENST00000487125.1:n.296-21C>A
NM_016188.4:c.760-21C>A	NP_057272.1:n.760-21C>A
XR_927476.1:n.867-21C>A
NR_134539.1:n.867-21C>A
NM_016188.5:c.760-21C>A MANE Select	NP_057272.1:n.760-21C>A
NR_134539.2:n.854-21C>A