Canonical Allele Identifier: CA107997252

Gene:

Linked Data

• dbSNP Id: rs1012220325
• MyVariant Identifiers: chr4:g.149669562C>T (hg19) ; chr4:g.148748410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148748410C>T , CM000666.2:g.148748410C>T	GRCh38
NC_000004.11:g.149669562C>T , CM000666.1:g.149669562C>T	GRCh37
NC_000004.10:g.149889012C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741441.1:n.1746-118347C>T