Canonical Allele Identifier: CA97374100

Gene:

Linked Data

• dbSNP Id: rs756876843
• MyVariant Identifiers: chr4:g.54938590C>A (hg19) ; chr4:g.54072423C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54072423C>A , CM000666.2:g.54072423C>A	GRCh38
NC_000004.11:g.54938590C>A , CM000666.1:g.54938590C>A	GRCh37
NC_000004.10:g.54633347C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000507166.5:c.1018-202502C>A	ENSP00000423325.1:n.1018-202502C>A