Canonical Allele Identifier: CA122896125

Gene:

Linked Data

• dbSNP Id: rs761132001
• MyVariant Identifiers: chr5:g.91518736G>A (hg19) ; chr5:g.92222919G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.92222919G>A , CM000667.2:g.92222919G>A	GRCh38
NC_000005.9:g.91518736G>A , CM000667.1:g.91518736G>A	GRCh37
NC_000005.8:g.91554492G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948565.1:n.394+18235G>A