Canonical Allele Identifier: CA823854220
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1260090511
gnomAD v4: 6-31200147-C-T
MyVariant Identifiers: chr6:g.31167924C>T (hg19) chr6:g.31200147C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200147C>T , CM000668.2:g.31200147C>T GRCh38
NC_000006.11:g.31167924C>T , CM000668.1:g.31167924C>T GRCh37
NC_000006.10:g.31275903C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.124-2225C>T
ENST00000414008.2:n.254C>T
ENST00000424675.1:c.44+1966C>T
NR_026791.1:n.124-2225C>T
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