Canonical Allele Identifier: CA783291329

Gene: ZNF627

Linked Data

• dbSNP Id: rs1176009843
• gnomAD v3: 19-11571651-G-A
• gnomAD v4: 19-11571651-G-A
• MyVariant Identifiers: chr19:g.11682466G>A (hg19) ; chr19:g.11571651G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11571651G>A , CM000681.2:g.11571651G>A	GRCh38
NC_000019.9:g.11682466G>A , CM000681.1:g.11682466G>A	GRCh37
NC_000019.8:g.11543466G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585493.5:c.-197-3599G>A	ENSP00000464997.1:n.-197-3599G>A
ENST00000588651.1:n.428-3599G>A
ENST00000593279.5:n.416-3599G>A