Canonical Allele Identifier: CA171706444

Gene:

Linked Data

• dbSNP Id: rs547615343
• gnomAD v2: 8-5764947-C-T
• gnomAD v3: 8-5907425-C-T
• gnomAD v4: 8-5907425-C-T
• MyVariant Identifiers: chr8:g.5764947C>T (hg19) ; chr8:g.5907425C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907425C>T , CM000670.2:g.5907425C>T	GRCh38
NC_000008.10:g.5764947C>T , CM000670.1:g.5764947C>T	GRCh37
NC_000008.9:g.5752355C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7694G>A
XR_941375.1:n.308-7694G>A
XR_941376.1:n.406-7694G>A
XR_941377.1:n.308-7694G>A
XR_941378.1:n.216-7694G>A
XR_001745765.1:n.308-7694G>A
XR_001745766.1:n.406-7694G>A
XR_001745767.1:n.216-7694G>A
XR_001745768.1:n.308-7694G>A
XR_941374.2:n.308-7694G>A
XR_941375.2:n.308-7694G>A