Canonical Allele Identifier: CA788493136

Gene:

Linked Data

• dbSNP Id: rs1411590325
• MyVariant Identifiers: chr4:g.145522590T>A (hg19) ; chr4:g.144601438T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601438T>A , CM000666.2:g.144601438T>A	GRCh38
NC_000004.11:g.145522590T>A , CM000666.1:g.145522590T>A	GRCh37
NC_000004.10:g.145742040T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649263.1:c.328-185460A>T	ENSP00000497507.1:n.328-185460A>T