Canonical Allele Identifier: CA20757733

Gene:

Linked Data

• dbSNP Id: rs978720265
• MyVariant Identifiers: chr1:g.34989280C>A (hg19) ; chr1:g.34523679C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.34523679C>A , CM000663.2:g.34523679C>A	GRCh38
NC_000001.10:g.34989280C>A , CM000663.1:g.34989280C>A	GRCh37
NC_000001.9:g.34761867C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947171.1:n.1073+23900G>T
XR_001737964.1:n.991+23900G>T