Canonical Allele Identifier: CA108745275

Gene:

Linked Data

• dbSNP Id: rs923084769
• gnomAD v2: 4-154864784-G-A
• gnomAD v3: 4-153943632-G-A
• gnomAD v4: 4-153943632-G-A
• MyVariant Identifiers: chr4:g.154864784G>A (hg19) ; chr4:g.153943632G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153943632G>A , CM000666.2:g.153943632G>A	GRCh38
NC_000004.11:g.154864784G>A , CM000666.1:g.154864784G>A	GRCh37
NC_000004.10:g.155084234G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001741892.1:n.1348-5189G>A