Canonical Allele Identifier: CA805749811

Gene:

Linked Data

• dbSNP Id: rs1355184612
• gnomAD v3: 5-152354508-A-G
• gnomAD v4: 5-152354508-A-G
• MyVariant Identifiers: chr5:g.151734069A>G (hg19) ; chr5:g.152354508A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.152354508A>G , CM000667.2:g.152354508A>G	GRCh38
NC_000005.9:g.151734069A>G , CM000667.1:g.151734069A>G	GRCh37
NC_000005.8:g.151714262A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_944433.1:n.196+16645A>G
XR_944433.2:n.197+16645A>G