Canonical Allele Identifier: CA1841175530
Gene:

Linked Data

dbSNP Id: rs17774966
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551359C>A , CM000671.2:g.25551359C>A GRCh38
NC_000009.11:g.25551357C>A , CM000671.1:g.25551357C>A GRCh37
NC_000009.10:g.25541357C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-787G>T
XR_929525.2:n.674-787G>T
Search 100 bp 5'
Search 100 bp 3'