Canonical Allele Identifier: CA437422067
Gene: CCDC50 HGNC NCBI

Linked Data

dbSNP Id: rs1225609392
MyVariant Identifiers: chr3:g.191092885T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375096T>G , CM000665.2:g.191375096T>G GRCh38
NC_000003.11:g.191092885T>G , CM000665.1:g.191092885T>G GRCh37
NC_000003.10:g.192575579T>G NCBI36
NG_008994.1:g.51012T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.483T>G MANE Select ENSP00000376249.4:p.Gly161=
ENST00000392456.4:c.448+5060T>G ENSP00000376250.4:n.448+5060T>G
ENST00000392455.7:c.448+5060T>G ENSP00000376249.3:n.448+5060T>G
ENST00000392456.3:c.483T>G ENSP00000376250.3:p.Gly161=
NM_174908.3:c.448+5060T>G NP_777568.1:n.448+5060T>G
NM_178335.2:c.483T>G NP_848018.1:p.Gly161=
XM_011512460.1:c.483T>G XP_011510762.1:p.Gly161=
NM_178335.3:c.483T>G MANE Select NP_848018.1:p.Gly161=
NM_174908.4:c.448+5060T>G NP_777568.1:n.448+5060T>G