Canonical Allele Identifier: CA15395804

Gene:

Linked Data

• dbSNP Id: rs10055544
• gnomAD v2: 5-91518721-G-A
• gnomAD v3: 5-92222904-G-A
• gnomAD v4: 5-92222904-G-A
• MyVariant Identifiers: chr5:g.91518721G>A (hg19) ; chr5:g.92222904G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.92222904G>A , CM000667.2:g.92222904G>A	GRCh38
NC_000005.9:g.91518721G>A , CM000667.1:g.91518721G>A	GRCh37
NC_000005.8:g.91554477G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948565.1:n.394+18220G>A