Canonical Allele Identifier: CA36160719

Gene:

Linked Data

• dbSNP Id: rs905449533
• MyVariant Identifiers: chr1:g.198469188T>A (hg19) ; chr1:g.198500058T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.198500058T>A , CM000663.2:g.198500058T>A	GRCh38
NC_000001.10:g.198469188T>A , CM000663.1:g.198469188T>A	GRCh37
NC_000001.9:g.196735811T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922398.1:n.679+19493A>T
XR_922398.2:n.341+19493A>T