Canonical Allele Identifier: CA841571712
Gene:

Linked Data

dbSNP Id: rs6965168
MyVariant Identifiers: chr7:g.68611984A>T (hg19) chr7:g.69146997A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146997A>T , CM000669.2:g.69146997A>T GRCh38
NC_000007.13:g.68611984A>T , CM000669.1:g.68611984A>T GRCh37
NC_000007.12:g.68249920A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-871T>A
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