Canonical Allele Identifier: CA166591537
Gene:

Linked Data

dbSNP Id: rs941238278
MyVariant Identifiers: chr7:g.123946309A>G (hg19) chr7:g.124306255A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306255A>G , CM000669.2:g.124306255A>G GRCh38
NC_000007.13:g.123946309A>G , CM000669.1:g.123946309A>G GRCh37
NC_000007.12:g.123733545A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-223A>G
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