Canonical Allele Identifier: CA555701597

Gene:

Linked Data

• dbSNP Id: rs1036898177
• gnomAD v2: 4-150901780-G-A
• gnomAD v3: 4-149980628-G-A
• gnomAD v4: 4-149980628-G-A
• MyVariant Identifiers: chr4:g.150901780G>A (hg19) ; chr4:g.149980628G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.149980628G>A , CM000666.2:g.149980628G>A	GRCh38
NC_000004.11:g.150901780G>A , CM000666.1:g.150901780G>A	GRCh37
NC_000004.10:g.151121230G>A	NCBI36