Canonical Allele Identifier: CA368543101
Gene: ACTL6B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100647038T>A , CM000669.2:g.100647038T>A GRCh38
NC_000007.13:g.100244661T>A , CM000669.1:g.100244661T>A GRCh37
NC_000007.12:g.100082597T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000160382.10:c.869A>T MANE Select ENSP00000160382.5:p.Tyr290Phe
ENST00000160382.9:c.869A>T ENSP00000160382.5:p.Tyr290Phe
ENST00000487125.1:n.431A>T
NM_016188.4:c.869A>T NP_057272.1:p.Tyr290Phe
XR_927476.1:n.976A>T
NR_134539.1:n.976A>T
NM_016188.5:c.869A>T MANE Select NP_057272.1:p.Tyr290Phe
NR_134539.2:n.963A>T