Canonical Allele Identifier: CA368543038
Gene: ACTL6B HGNC NCBI

Linked Data

dbSNP Id: rs149325579

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100647025G>C , CM000669.2:g.100647025G>C GRCh38
NC_000007.13:g.100244648G>C , CM000669.1:g.100244648G>C GRCh37
NC_000007.12:g.100082584G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000160382.10:c.882C>G MANE Select ENSP00000160382.5:p.Tyr294Ter
ENST00000160382.9:c.882C>G ENSP00000160382.5:p.Tyr294Ter
ENST00000487125.1:n.444C>G
NM_016188.4:c.882C>G NP_057272.1:p.Tyr294Ter
XR_927476.1:n.989C>G
NR_134539.1:n.989C>G
NM_016188.5:c.882C>G MANE Select NP_057272.1:p.Tyr294Ter
NR_134539.2:n.976C>G