Canonical Allele Identifier: CA15157274
Gene:

Linked Data

dbSNP Id: rs2667026
gnomAD v2: 2-160921555-G-A
gnomAD v3: 2-160065044-G-A
gnomAD v4: 2-160065044-G-A
MyVariant Identifiers: chr2:g.160921555G>A (hg19) chr2:g.160065044G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.160065044G>A , CM000664.2:g.160065044G>A GRCh38
NC_000002.11:g.160921555G>A , CM000664.1:g.160921555G>A GRCh37
NC_000002.10:g.160629801G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923525.1:n.1038+4091G>A
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