Canonical Allele Identifier: CA136833616
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1055596485
gnomAD v2: 6-31167876-A-G
gnomAD v3: 6-31200099-A-G
gnomAD v4: 6-31200099-A-G
MyVariant Identifiers: chr6:g.31167876A>G (hg19) chr6:g.31200099A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200099A>G , CM000668.2:g.31200099A>G GRCh38
NC_000006.11:g.31167876A>G , CM000668.1:g.31167876A>G GRCh37
NC_000006.10:g.31275855A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2217A>G
ENST00000414008.2:n.206A>G
ENST00000424675.1:c.44+1918A>G
NR_026791.1:n.123+2217A>G
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