Canonical Allele Identifier: CA191701702
Gene:

Linked Data

dbSNP Id: rs753110183
MyVariant Identifiers: chr9:g.25551389A>G (hg19) chr9:g.25551391A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551391A>G , CM000671.2:g.25551391A>G GRCh38
NC_000009.11:g.25551389A>G , CM000671.1:g.25551389A>G GRCh37
NC_000009.10:g.25541389A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-819T>C
XR_929525.2:n.674-819T>C
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