Canonical Allele Identifier: CA2677946783
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200047-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200047T>C , CM000668.2:g.31200047T>C GRCh38
NC_000006.11:g.31167824T>C , CM000668.1:g.31167824T>C GRCh37
NC_000006.10:g.31275803T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2165T>C
ENST00000414008.2:n.154T>C
ENST00000424675.1:c.44+1866T>C
NR_026791.1:n.123+2165T>C
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