Canonical Allele Identifier: CA838949480

Gene:

Linked Data

• dbSNP Id: rs1488663981
• MyVariant Identifiers: chr7:g.46072666G>A (hg19) ; chr7:g.46033068G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.46033068G>A , CM000669.2:g.46033068G>A	GRCh38
NC_000007.13:g.46072666G>A , CM000669.1:g.46072666G>A	GRCh37
NC_000007.12:g.46039191G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745203.1:n.1270-3550G>A