Canonical Allele Identifier: CA107754092

Gene:

Linked Data

• dbSNP Id: rs956482702
• MyVariant Identifiers: chr4:g.145522718A>C (hg19) ; chr4:g.144601566A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601566A>C , CM000666.2:g.144601566A>C	GRCh38
NC_000004.11:g.145522718A>C , CM000666.1:g.145522718A>C	GRCh37
NC_000004.10:g.145742168A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-185588T>G	ENSP00000497507.1:n.328-185588T>G