Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA449627504

Gene: HCG27 HGNC NCBI

Linked Data

gnomAD v4: 6-31200171-G-A

MyVariant Identifiers: chr6:g.31167948G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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

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