Canonical Allele Identifier: CA823854208
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs1257065639
gnomAD v4: 6-31200122-G-A
MyVariant Identifiers: chr6:g.31167899G>A (hg19) chr6:g.31200122G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200122G>A , CM000668.2:g.31200122G>A GRCh38
NC_000006.11:g.31167899G>A , CM000668.1:g.31167899G>A GRCh37
NC_000006.10:g.31275878G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2240G>A
ENST00000414008.2:n.229G>A
ENST00000424675.1:c.44+1941G>A
NR_026791.1:n.123+2240G>A
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