Canonical Allele Identifier: CA136833612

Gene: HCG27

Linked Data

• dbSNP Id: rs950957146
• gnomAD v3: 6-31200087-T-G
• gnomAD v4: 6-31200087-T-G
• MyVariant Identifiers: chr6:g.31167864T>G (hg19) ; chr6:g.31200087T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31200087T>G , CM000668.2:g.31200087T>G	GRCh38
NC_000006.11:g.31167864T>G , CM000668.1:g.31167864T>G	GRCh37
NC_000006.10:g.31275843T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383331.4:c.123+2205T>G
ENST00000414008.2:n.194T>G
ENST00000424675.1:c.44+1906T>G
NR_026791.1:n.123+2205T>G