Canonical Allele Identifier: CA579869969

Gene:

Linked Data

• dbSNP Id: rs1193965986
• gnomAD v2: 8-5764594-A-C
• gnomAD v3: 8-5907072-A-C
• gnomAD v4: 8-5907072-A-C
• MyVariant Identifiers: chr8:g.5764594A>C (hg19) ; chr8:g.5907072A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907072A>C , CM000670.2:g.5907072A>C	GRCh38
NC_000008.10:g.5764594A>C , CM000670.1:g.5764594A>C	GRCh37
NC_000008.9:g.5752002A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7341T>G
XR_941375.1:n.308-7341T>G
XR_941376.1:n.406-7341T>G
XR_941377.1:n.308-7341T>G
XR_941378.1:n.216-7341T>G
XR_001745765.1:n.308-7341T>G
XR_001745766.1:n.406-7341T>G
XR_001745767.1:n.216-7341T>G
XR_001745768.1:n.308-7341T>G
XR_941374.2:n.308-7341T>G
XR_941375.2:n.308-7341T>G