Canonical Allele Identifier: CA026384
Gene:
ClinVar RCV:
RCV000013960
ClinVar Variation:
13085
dbSNP:
387906520
gnomAD v4:
chr13-48303724-G-T
MyVariant.info:
GRCh38 chr13:g.48303724G>T
GRCh37 chr13:g.48877860G>T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303724G>T , CM000675.2:g.48303724G>T GRCh38
NC_000013.10:g.48877860G>T , CM000675.1:g.48877860G>T GRCh37
NC_000013.9:g.47775861G>T NCBI36
NG_009009.1:g.4978G>T , LRG_517:g.4978G>T
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