Canonical Allele Identifier: CA122896191

Gene:

Linked Data

• dbSNP Id: rs1046321207
• gnomAD v2: 5-91518824-T-A
• gnomAD v3: 5-92223007-T-A
• gnomAD v4: 5-92223007-T-A
• MyVariant Identifiers: chr5:g.91518824T>A (hg19) ; chr5:g.92223007T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.92223007T>A , CM000667.2:g.92223007T>A	GRCh38
NC_000005.9:g.91518824T>A , CM000667.1:g.91518824T>A	GRCh37
NC_000005.8:g.91554580T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948565.1:n.394+18323T>A