Canonical Allele Identifier: CA36798920

Gene:

Linked Data

• dbSNP Id: rs1005575157
• MyVariant Identifiers: chr1:g.211553003G>A (hg19) ; chr1:g.211379661G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.211379661G>A , CM000663.2:g.211379661G>A	GRCh38
NC_000001.10:g.211553003G>A , CM000663.1:g.211553003G>A	GRCh37
NC_000001.9:g.209619626G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738446.1:n.291+2534C>T