Canonical Allele Identifier: CA725880999
Gene:

Linked Data

dbSNP Id: rs1414659502
MyVariant Identifiers: chr16:g.9675160G>A (hg19) chr16:g.9581303G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9581303G>A , CM000678.2:g.9581303G>A GRCh38
NC_000016.9:g.9675160G>A , CM000678.1:g.9675160G>A GRCh37
NC_000016.8:g.9582661G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_429665.2:n.1065+14713G>A
XR_001752073.1:n.1766+14713G>A
XR_001752074.1:n.650+14713G>A
XR_001752075.1:n.740+14713G>A
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