Canonical Allele Identifier: CA136833603
Gene: HCG27 HGNC NCBI

Linked Data

dbSNP Id: rs964812739
MyVariant Identifiers: chr6:g.31167837G>A (hg19) chr6:g.31200060G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31200060G>A , CM000668.2:g.31200060G>A GRCh38
NC_000006.11:g.31167837G>A , CM000668.1:g.31167837G>A GRCh37
NC_000006.10:g.31275816G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000383331.4:c.123+2178G>A
ENST00000414008.2:n.167G>A
ENST00000424675.1:c.44+1879G>A
NR_026791.1:n.123+2178G>A
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