Canonical Allele Identifier: CA813569878

Gene:

Linked Data

• dbSNP Id: rs1465263419
• MyVariant Identifiers: chr5:g.69345349G>A (hg19) ; chr5:g.70049522G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70049522G>A , CM000667.2:g.70049522G>A	GRCh38
NC_000005.9:g.69345349G>A , CM000667.1:g.69345349G>A	GRCh37
NC_000005.8:g.69381105G>A	NCBI36
NG_008728.1:g.5000G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_948432.1:n.1054+61518G>A