Canonical Allele Identifier: CA2718860992
Gene:

Linked Data

dbSNP Id: rs1279796692
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551158C>T , CM000671.2:g.25551158C>T GRCh38
NC_000009.11:g.25551156C>T , CM000671.1:g.25551156C>T GRCh37
NC_000009.10:g.25541156C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-586G>A
XR_929525.2:n.674-586G>A
Search 100 bp 5'
Search 100 bp 3'