Canonical Allele Identifier: CA820839161

Gene:

Linked Data

• dbSNP Id: rs1299707269
• MyVariant Identifiers: chr6:g.151954704_151954705insA (hg19) ; chr6:g.151633569_151633570insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633570dup , CM000668.2:g.151633570dup	GRCh38
NC_000006.11:g.151954705dup , CM000668.1:g.151954705dup	GRCh37
NC_000006.10:g.151996398dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3588dup