Canonical Allele Identifier: CA729343639

Gene:

Linked Data

• dbSNP Id: rs1320386733
• MyVariant Identifiers: chr1:g.193090830_193090831insA (hg19) ; chr1:g.193121700_193121701insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121701dup , CM000663.2:g.193121701dup	GRCh38
NC_000001.10:g.193090831dup , CM000663.1:g.193090831dup	GRCh37
NC_000001.9:g.191357454dup	NCBI36
NG_012691.1:g.4744dup , LRG_507:g.4744dup

Transcript Alleles

HGVS	Amino-acid Change
XR_001738350.1:n.1956dup