Canonical Allele Identifier: CA74805336

Gene:

Linked Data

• dbSNP Id: rs770513520
• MyVariant Identifiers: chr3:g.53091214G>A (hg19) ; chr3:g.53057198G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53057198G>A , CM000665.2:g.53057198G>A	GRCh38
NC_000003.11:g.53091214G>A , CM000665.1:g.53091214G>A	GRCh37
NC_000003.10:g.53066254G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607203.1:c.318-9959C>T
ENST00000607283.5:c.465-13944C>T
ENST00000607495.5:c.447+20490C>T