Canonical Allele Identifier: CA449627505
Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200171-G-C
MyVariant Identifiers: chr6:g.31167948G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200171G>C , CM000668.2:g.31200171G>C GRCh38
NC_000006.11:g.31167948G>C , CM000668.1:g.31167948G>C GRCh37
NC_000006.10:g.31275927G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383331.4:c.124-2201G>C
ENST00000414008.2:n.278G>C
ENST00000424675.1:c.44+1990G>C
NR_026791.1:n.124-2201G>C
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