Canonical Allele Identifier: CA15473001

Gene:

Linked Data

• dbSNP Id: rs11753383
• gnomAD v2: 6-151954659-G-A
• gnomAD v3: 6-151633524-G-A
• gnomAD v4: 6-151633524-G-A
• MyVariant Identifiers: chr6:g.151954659G>A (hg19) ; chr6:g.151633524G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633524G>A , CM000668.2:g.151633524G>A	GRCh38
NC_000006.11:g.151954659G>A , CM000668.1:g.151954659G>A	GRCh37
NC_000006.10:g.151996352G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3542G>A