Canonical Allele Identifier: CA97374097

Gene:

Linked Data

• dbSNP Id: rs963059729
• MyVariant Identifiers: chr4:g.54938568A>G (hg19) ; chr4:g.54072401A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.54072401A>G , CM000666.2:g.54072401A>G	GRCh38
NC_000004.11:g.54938568A>G , CM000666.1:g.54938568A>G	GRCh37
NC_000004.10:g.54633325A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000507166.5:c.1018-202524A>G	ENSP00000423325.1:n.1018-202524A>G