Canonical Allele Identifier: CA310250204
Gene:

Linked Data

dbSNP Id: rs17634917
gnomAD v2: 19-56265664-A-G
gnomAD v3: 19-55754298-A-G
gnomAD v4: 19-55754298-A-G
MyVariant Identifiers: chr19:g.56265664A>G (hg19) chr19:g.55754298A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55754298A>G , CM000681.2:g.55754298A>G GRCh38
NC_000019.9:g.56265664A>G , CM000681.1:g.56265664A>G GRCh37
NC_000019.8:g.60957476A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936081.1:n.167A>G
XR_936081.2:n.226A>G
Search 100 bp 5'
Search 100 bp 3'