Canonical Allele Identifier: CA107754154

Gene:

Linked Data

• dbSNP Id: rs942251971
• MyVariant Identifiers: chr4:g.145522779T>G (hg19) ; chr4:g.144601627T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144601627T>G , CM000666.2:g.144601627T>G	GRCh38
NC_000004.11:g.145522779T>G , CM000666.1:g.145522779T>G	GRCh37
NC_000004.10:g.145742229T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649263.1:c.328-185649A>C	ENSP00000497507.1:n.328-185649A>C