Canonical Allele Identifier: CA107753937

Gene:

Linked Data

• dbSNP Id: rs889778092
• MyVariant Identifiers: chr4:g.145522549T>C (hg19) ; chr4:g.144601397T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601397T>C , CM000666.2:g.144601397T>C	GRCh38
NC_000004.11:g.145522549T>C , CM000666.1:g.145522549T>C	GRCh37
NC_000004.10:g.145741999T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-185419A>G	ENSP00000497507.1:n.328-185419A>G