Canonical Allele Identifier: CA175154062
Gene:

Linked Data

dbSNP Id: rs1037696346
MyVariant Identifiers: chr8:g.33665933T>A (hg19) chr8:g.33808415T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808415T>A , CM000670.2:g.33808415T>A GRCh38
NC_000008.10:g.33665933T>A , CM000670.1:g.33665933T>A GRCh37
NC_000008.9:g.33785475T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11979T>A
XR_002956701.1:n.240+11979T>A
Search 100 bp 5'
Search 100 bp 3'