Canonical Allele Identifier: CA107753963

Gene:

Linked Data

• dbSNP Id: rs181726275
• gnomAD v2: 4-145522585-G-A
• gnomAD v3: 4-144601433-G-A
• gnomAD v4: 4-144601433-G-A
• MyVariant Identifiers: chr4:g.145522585G>A (hg19) ; chr4:g.144601433G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601433G>A , CM000666.2:g.144601433G>A	GRCh38
NC_000004.11:g.145522585G>A , CM000666.1:g.145522585G>A	GRCh37
NC_000004.10:g.145742035G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-185455C>T	ENSP00000497507.1:n.328-185455C>T