Canonical Allele Identifier: CA1619157150

Gene:

Linked Data

• dbSNP Id: rs1761789508

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439996_31439997insG , CM000668.2:g.31439996_31439997insG	GRCh38
NC_000006.11:g.31407773_31407774insG , CM000668.1:g.31407773_31407774insG	GRCh37
NC_000006.10:g.31515752_31515753insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.110_111insC