Canonical Allele Identifier: CA160479213
Gene:

Linked Data

dbSNP Id: rs748824983
MyVariant Identifiers: chr7:g.68612051C>G (hg19) chr7:g.69147064C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69147064C>G , CM000669.2:g.69147064C>G GRCh38
NC_000007.13:g.68612051C>G , CM000669.1:g.68612051C>G GRCh37
NC_000007.12:g.68249987C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-938G>C
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