Canonical Allele Identifier: CA74805305

Gene:

Linked Data

• dbSNP Id: rs936671928
• MyVariant Identifiers: chr3:g.53091159C>T (hg19) ; chr3:g.53057143C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53057143C>T , CM000665.2:g.53057143C>T	GRCh38
NC_000003.11:g.53091159C>T , CM000665.1:g.53091159C>T	GRCh37
NC_000003.10:g.53066199C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607203.1:c.318-9904G>A
ENST00000607283.5:c.465-13889G>A
ENST00000607495.5:c.447+20545G>A