Canonical Allele Identifier: CA161196172
Gene: CCDC146 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12540771

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.77133634A>G , CM000669.2:g.77133634A>G GRCh38
NC_000007.13:g.76762951A>G , CM000669.1:g.76762951A>G GRCh37
NC_000007.12:g.76600887A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_020879.2:c.-12+10902A>G VV NP_065930.2:p.=
XR_927691.1:n.48-4908T>C
NM_020879.3:c.-12+10902A>G VV MANE Preferred NP_065930.2:p.=
ENST00000285871.4:c.-12+10902A>G ENSP00000285871.4:p.=
ENST00000415750.5:c.-12+11166A>G ENSP00000388649.1:p.=