Canonical Allele Identifier: CA844313402
Gene:

Linked Data

dbSNP Id: rs1343736785
MyVariant Identifiers: chr7:g.97017663A>G (hg19) chr7:g.97388351A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388351A>G , CM000669.2:g.97388351A>G GRCh38
NC_000007.13:g.97017663A>G , CM000669.1:g.97017663A>G GRCh37
NC_000007.12:g.96855599A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59704T>C
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