Canonical Allele Identifier: CA99746701

Gene:

Linked Data

• dbSNP Id: rs1050208525
• MyVariant Identifiers: chr4:g.75170142C>T (hg19) ; chr4:g.74304425C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74304425C>T , CM000666.2:g.74304425C>T	GRCh38
NC_000004.11:g.75170142C>T , CM000666.1:g.75170142C>T	GRCh37
NC_000004.10:g.75389006C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938877.1:n.120-25647G>A
XR_938877.2:n.126-25647G>A