Canonical Allele Identifier: CA1092269972

Gene:

Linked Data

• dbSNP Id: rs1773161987
• gnomAD v3: 6-98102504-T-TC
• gnomAD v4: 6-98102504-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98102504_98102505insC , CM000668.2:g.98102504_98102505insC	GRCh38
NC_000006.11:g.98550380_98550381insC , CM000668.1:g.98550380_98550381insC	GRCh37
NC_000006.10:g.98657101_98657102insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245563.2:n.456+3234_456+3235insC
XR_942809.1:n.456+3234_456+3235insC