Canonical Allele Identifier: CA551566754
Gene: SRD5A3 HGNC NCBI

Linked Data

dbSNP Id: rs201174794
gnomAD v2: 4-56212370-G-GCGCGTCCCCGCCCCGCGCCGCGTCCCCGCCCCGCGC
gnomAD v3: 4-55346203-G-GCGCGTCCCCGCCCCGCGCCGCGTCCCCGCCCCGCGC
gnomAD v4: 4-55346203-G-GCGCGTCCCCGCCCCGCGCCGCGTCCCCGCCCCGCGC
MyVariant Identifiers: chr4:g.56212370_56212371insCGCGTCCCCGCCCCGCGCCGCGTCCCCGCCCCGCGC (hg19) chr4:g.55346203_55346204insCGCGTCCCCGCCCCGCGCCGCGTCCCCGCCCCGCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55346227_55346228insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC , CM000666.2:g.55346227_55346228insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC GRCh38
NC_000004.11:g.56212394_56212395insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC , CM000666.1:g.56212394_56212395insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC GRCh37
NC_000004.10:g.55907151_55907152insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC NCBI36
NG_028230.1:g.5007_5008insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000264228.8:c.-110_-109insCCCGCCCCGCGCCGCGTCCCCGCCCCGCGCCGCGTC ENSP00000264228.4:n.-110_-109insCCCGCCCCGCGCCGCGTCCCCGCCCCGCG...
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