Canonical Allele Identifier: CA37327617

Gene:

Linked Data

• dbSNP Id: rs1047313166
• MyVariant Identifiers: chr1:g.213855617_213855618insT (hg19) ; chr1:g.213682274_213682275insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.213682281dup , CM000663.2:g.213682281dup	GRCh38
NC_000001.10:g.213855624dup , CM000663.1:g.213855624dup	GRCh37
NC_000001.9:g.211922247dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738463.1:n.601-49136dup
XR_001738464.1:n.426-49136dup