Canonical Allele Identifier: CA12010408
Gene:

Linked Data

dbSNP Id: rs3091338
gnomAD v2: 5-131402738-C-T
gnomAD v3: 5-132067045-C-T
gnomAD v4: 5-132067045-C-T
MyVariant Identifiers: chr5:g.131402738C>T (hg19) chr5:g.132067045C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132067045C>T , CM000667.2:g.132067045C>T GRCh38
NC_000005.9:g.131402738C>T , CM000667.1:g.131402738C>T GRCh37
NC_000005.8:g.131430637C>T NCBI36
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