Canonical Allele Identifier: CA2497214502
Gene: ACTL6B HGNC NCBI

Linked Data

dbSNP Id: rs1803836495

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100647024dup , CM000669.2:g.100647024dup GRCh38
NC_000007.13:g.100244647dup , CM000669.1:g.100244647dup GRCh37
NC_000007.12:g.100082583dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000160382.10:c.884dup MANE Select ENSP00000160382.5:p.Ala296ArgfsTer8
ENST00000160382.9:c.884dup ENSP00000160382.5:p.Ala296ArgfsTer8
ENST00000487125.1:n.446dup
NM_016188.4:c.884dup NP_057272.1:p.Ala296ArgfsTer8
XR_927476.1:n.991dup
NR_134539.1:n.991dup
NM_016188.5:c.884dup MANE Select NP_057272.1:p.Ala296ArgfsTer8
NR_134539.2:n.978dup