Canonical Allele Identifier: CA475494035
Gene: ACTN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.66327846C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560375C>T , CM000673.2:g.66560375C>T GRCh38
NC_000011.9:g.66327846C>T , CM000673.1:g.66327846C>T GRCh37
NC_000011.8:g.66084422C>T NCBI36
NG_013304.2:g.18456C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1677+64C>T MANE Select ENSP00000426797.1:n.1677+64C>T
ENST00000502692.5:c.1806+64C>T ENSP00000422007.1:n.1806+64C>T
ENST00000513398.1:c.1677+64C>T ENSP00000426797.1:n.1677+64C>T
NM_001104.3:c.1677+64C>T NP_001095.2:n.1677+64C>T
NM_001258371.2:c.1806+64C>T NP_001245300.2:n.1806+64C>T
NM_001104.4:c.1677+64C>T MANE Select NP_001095.2:n.1677+64C>T
NM_001258371.3:c.1806+64C>T NP_001245300.2:n.1806+64C>T