Canonical Allele Identifier: CA571116552

Gene:

Linked Data

• dbSNP Id: rs1210687998
• gnomAD v2: 6-151954772-G-GC
• gnomAD v3: 6-151633637-G-GC
• gnomAD v4: 6-151633637-G-GC
• MyVariant Identifiers: chr6:g.151954772_151954773insC (hg19) ; chr6:g.151633637_151633638insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633638dup , CM000668.2:g.151633638dup	GRCh38
NC_000006.11:g.151954773dup , CM000668.1:g.151954773dup	GRCh37
NC_000006.10:g.151996466dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3656dup