Canonical Allele Identifier: CA729866072

Gene:

Linked Data

• dbSNP Id: rs1328952306
• MyVariant Identifiers: chr1:g.198469171G>A (hg19) ; chr1:g.198500041G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198500041G>A , CM000663.2:g.198500041G>A	GRCh38
NC_000001.10:g.198469171G>A , CM000663.1:g.198469171G>A	GRCh37
NC_000001.9:g.196735794G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_922398.1:n.679+19510C>T
XR_922398.2:n.341+19510C>T