Canonical Allele Identifier: CA4387099

Gene: ACTL6B

Linked Data

• dbSNP Id: rs776351615
• ExAC: 7:100244498 C / T
• gnomAD v2: 7-100244498-C-T
• gnomAD v3: 7-100646875-C-T
• gnomAD v4: 7-100646875-C-T
• MyVariant Identifiers: chr7:g.100244498C>T (hg19) ; chr7:g.100646875C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100646875C>T , CM000669.2:g.100646875C>T	GRCh38
NC_000007.13:g.100244498C>T , CM000669.1:g.100244498C>T	GRCh37
NC_000007.12:g.100082434C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000160382.10:c.937-44G>A MANE Select	ENSP00000160382.5:n.937-44G>A
ENST00000160382.9:c.937-44G>A	ENSP00000160382.5:n.937-44G>A
ENST00000487125.1:n.499-44G>A
NM_016188.4:c.937-44G>A	NP_057272.1:n.937-44G>A
XR_927476.1:n.1044-44G>A
NR_134539.1:n.1044-44G>A
NM_016188.5:c.937-44G>A MANE Select	NP_057272.1:n.937-44G>A
NR_134539.2:n.1031-44G>A