Canonical Allele Identifier: CA815487981

Gene:

Linked Data

• dbSNP Id: rs1205542385
• MyVariant Identifiers: chr5:g.91518586C>T (hg19) ; chr5:g.92222769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.92222769C>T , CM000667.2:g.92222769C>T	GRCh38
NC_000005.9:g.91518586C>T , CM000667.1:g.91518586C>T	GRCh37
NC_000005.8:g.91554342C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948565.1:n.394+18085C>T