Canonical Allele Identifier: CA31174458

Gene:

Linked Data

• dbSNP Id: rs1001990198
• gnomAD v2: 1-157674803-G-A
• gnomAD v3: 1-157705013-G-A
• gnomAD v4: 1-157705013-G-A
• MyVariant Identifiers: chr1:g.157674803G>A (hg19) ; chr1:g.157705013G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.157705013G>A , CM000663.2:g.157705013G>A	GRCh38
NC_000001.10:g.157674803G>A , CM000663.1:g.157674803G>A	GRCh37
NC_000001.9:g.155941427G>A	NCBI36
NG_023241.1:g.845C>T