Canonical Allele Identifier: CA107754168

Gene:

Linked Data

• dbSNP Id: rs934176549
• gnomAD v2: 4-145522789-C-T
• gnomAD v3: 4-144601637-C-T
• gnomAD v4: 4-144601637-C-T
• MyVariant Identifiers: chr4:g.145522789C>T (hg19) ; chr4:g.144601637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601637C>T , CM000666.2:g.144601637C>T	GRCh38
NC_000004.11:g.145522789C>T , CM000666.1:g.145522789C>T	GRCh37
NC_000004.10:g.145742239C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649263.1:c.328-185659G>A	ENSP00000497507.1:n.328-185659G>A