Canonical Allele Identifier: CA163625033
Gene:

Linked Data

dbSNP Id: rs1022070859
MyVariant Identifiers: chr7:g.97017668C>T (hg19) chr7:g.97388356C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388356C>T , CM000669.2:g.97388356C>T GRCh38
NC_000007.13:g.97017668C>T , CM000669.1:g.97017668C>T GRCh37
NC_000007.12:g.96855604C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59709G>A
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