Canonical Allele Identifier: CA36160712
Gene:

Linked Data

dbSNP Id: rs761517788
MyVariant Identifiers: chr1:g.198469146C>A (hg19) chr1:g.198500016C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198500016C>A , CM000663.2:g.198500016C>A GRCh38
NC_000001.10:g.198469146C>A , CM000663.1:g.198469146C>A GRCh37
NC_000001.9:g.196735769C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922398.1:n.679+19535G>T
XR_922398.2:n.341+19535G>T
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