Canonical Allele Identifier: CA788493147

Gene:

Linked Data

• dbSNP Id: rs533522231
• gnomAD v3: 4-144601466-G-A
• gnomAD v4: 4-144601466-G-A
• MyVariant Identifiers: chr4:g.145522618G>A (hg19) ; chr4:g.144601466G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601466G>A , CM000666.2:g.144601466G>A	GRCh38
NC_000004.11:g.145522618G>A , CM000666.1:g.145522618G>A	GRCh37
NC_000004.10:g.145742068G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-185488C>T	ENSP00000497507.1:n.328-185488C>T