Canonical Allele Identifier: CA11001492
Gene:

Linked Data

dbSNP Id: rs3755132
gnomAD v2: 2-15729820-T-G
gnomAD v3: 2-15589696-T-G
gnomAD v4: 2-15589696-T-G
MyVariant Identifiers: chr2:g.15729820T>G (hg19) chr2:g.15589696T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15589696T>G , CM000664.2:g.15589696T>G GRCh38
NC_000002.11:g.15729820T>G , CM000664.1:g.15729820T>G GRCh37
NC_000002.10:g.15647271T>G NCBI36
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