Canonical Allele Identifier: CA906503831

Gene:

Linked Data

• dbSNP Id: rs1315535988
• MyVariant Identifiers: chr3:g.34962830C>T (hg19) ; chr3:g.34921338C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.34921338C>T , CM000665.2:g.34921338C>T	GRCh38
NC_000003.11:g.34962830C>T , CM000665.1:g.34962830C>T	GRCh37
NC_000003.10:g.34937834C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110817.1:n.207-41872G>A