Canonical Allele Identifier: CA573583322

Gene:

Linked Data

• dbSNP Id: rs1437359140
• gnomAD v2: 7-26645374-A-G
• MyVariant Identifiers: chr7:g.26645374A>G (hg19) ; chr7:g.26605755A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26605755A>G , CM000669.2:g.26605755A>G	GRCh38
NC_000007.13:g.26645374A>G , CM000669.1:g.26645374A>G	GRCh37
NC_000007.12:g.26611899A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927131.1:n.1118-6385T>C
XR_927131.2:n.1186-6385T>C