Canonical Allele Identifier: CA107754179

Gene:

Linked Data

• dbSNP Id: rs941303441
• MyVariant Identifiers: chr4:g.145522815G>T (hg19) ; chr4:g.144601663G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601663G>T , CM000666.2:g.144601663G>T	GRCh38
NC_000004.11:g.145522815G>T , CM000666.1:g.145522815G>T	GRCh37
NC_000004.10:g.145742265G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-185685C>A	ENSP00000497507.1:n.328-185685C>A