Canonical Allele Identifier: CA10635850
Gene: ACTC1 HGNC NCBI
GJD2-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 315661
dbSNP Id: rs886051068

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.34789191T>A , CM000677.2:g.34789191T>A GRCh38
NC_000015.9:g.35081392T>A , CM000677.1:g.35081392T>A GRCh37
NC_000015.8:g.32868684T>A NCBI36
NG_007553.1:g.11536A>T , LRG_388:g.11536A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000290378.4:c.*1221A>T (ACTC1) ENSP00000290378.4:n.*1221A>T
NM_005159.4:c.*1221A>T , LRG_388t1:c.*1221A>T (ACTC1) NP_005150.1:n.*1221A>T
NR_120329.1:n.299+11760T>A (GJD2-DT)