Canonical Allele Identifier: CA862568271
Gene:

Linked Data

dbSNP Id: rs1192351764
MyVariant Identifiers: chr9:g.25551519A>T (hg19) chr9:g.25551521A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551521A>T , CM000671.2:g.25551521A>T GRCh38
NC_000009.11:g.25551519A>T , CM000671.1:g.25551519A>T GRCh37
NC_000009.10:g.25541519A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-949T>A
XR_929525.2:n.674-949T>A
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