Canonical Allele Identifier: CA13720823
Gene: RERG HGNC NCBI

Linked Data

dbSNP Id: rs12311304
gnomAD v2: 12-15389637-T-C
gnomAD v3: 12-15236703-T-C
gnomAD v4: 12-15236703-T-C
MyVariant Identifiers: chr12:g.15389637T>C (hg19) chr12:g.15236703T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.15236703T>C , CM000674.2:g.15236703T>C GRCh38
NC_000012.11:g.15389637T>C , CM000674.1:g.15389637T>C GRCh37
NC_000012.10:g.15280904T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393736.3:c.-114-19100A>G ENSP00000440887.1:n.-114-19100A>G
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