Canonical Allele Identifier: CA663550285

Gene:

Linked Data

• dbSNP Id: rs1329293333
• MyVariant Identifiers: chr10:g.29364701A>T (hg19) ; chr10:g.29075772A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.29075772A>T , CM000672.2:g.29075772A>T	GRCh38
NC_000010.10:g.29364701A>T , CM000672.1:g.29364701A>T	GRCh37
NC_000010.9:g.29404707A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001747284.1:n.127-3720A>T