Canonical Allele Identifier: CA475494419
Gene: ACTN3 HGNC NCBI

Linked Data

dbSNP Id: rs1857737113
MyVariant Identifiers: chr11:g.66328172C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66560701C>T , CM000673.2:g.66560701C>T GRCh38
NC_000011.9:g.66328172C>T , CM000673.1:g.66328172C>T GRCh37
NC_000011.8:g.66084748C>T NCBI36
NG_013304.2:g.18782C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513398.2:c.1806C>T MANE Select ENSP00000426797.1:p.Ser602=
ENST00000502692.5:c.1935C>T ENSP00000422007.1:p.Ser645=
ENST00000513398.1:c.1806C>T ENSP00000426797.1:p.Ser602=
NM_001104.3:c.1806C>T NP_001095.2:p.Ser602=
NM_001258371.2:c.1935C>T NP_001245300.2:p.Ser645=
NM_001104.4:c.1806C>T MANE Select NP_001095.2:p.Ser602=
NM_001258371.3:c.1935C>T NP_001245300.2:p.Ser645=