Canonical Allele Identifier: CA165047076

Gene:

Linked Data

• dbSNP Id: rs892127959
• MyVariant Identifiers: chr7:g.112628386G>A (hg19) ; chr7:g.112988331G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.112988331G>A , CM000669.2:g.112988331G>A	GRCh38
NC_000007.13:g.112628386G>A , CM000669.1:g.112628386G>A	GRCh37
NC_000007.12:g.112415622G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110162.1:n.77-1667C>T