Canonical Allele Identifier: CA47693381
Gene:

Linked Data

dbSNP Id: rs138517359
gnomAD v3: 2-52722525-C-T
gnomAD v4: 2-52722525-C-T
MyVariant Identifiers: chr2:g.52949663C>T (hg19) chr2:g.52722525C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722525C>T , CM000664.2:g.52722525C>T GRCh38
NC_000002.11:g.52949663C>T , CM000664.1:g.52949663C>T GRCh37
NC_000002.10:g.52803167C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.732G>A
Search 100 bp 5'
Search 100 bp 3'