Canonical Allele Identifier: CA573843897

Gene:

Linked Data

• gnomAD v2: 7-41821973-A-G
• MyVariant Identifiers: chr7:g.41821973A>G (hg19) ; chr7:g.41782375A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41782375A>G , CM000669.2:g.41782375A>G	GRCh38
NC_000007.13:g.41821973A>G , CM000669.1:g.41821973A>G	GRCh37
NC_000007.12:g.41788498A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745185.1:n.964+46661A>G
XR_001745186.1:n.954+46671A>G