Canonical Allele Identifier: CA1100722848
Gene: URGCP-MRPS24 HGNC NCBI

Linked Data

dbSNP Id: rs2095840309
gnomAD v3: 7-43871208-A-G
gnomAD v4: 7-43871208-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.43871208A>G , CM000669.2:g.43871208A>G GRCh38
NC_000007.13:g.43910807A>G , CM000669.1:g.43910807A>G GRCh37
NC_000007.12:g.43877332A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000603700.1:c.176-1832T>C ENSP00000473871.1:n.176-1832T>C
NM_001204871.1:c.176-1832T>C NP_001191800.1:n.176-1832T>C
NM_001204871.2:c.176-1832T>C NP_001191800.1:n.176-1832T>C