Canonical Allele Identifier: CA154890387
Gene:

Linked Data

dbSNP Id: rs763231773
MyVariant Identifiers: chr7:g.17997593A>G (hg19) chr7:g.17957970A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957970A>G , CM000669.2:g.17957970A>G GRCh38
NC_000007.13:g.17997593A>G , CM000669.1:g.17997593A>G GRCh37
NC_000007.12:g.17964118A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-700A>G
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Search 100 bp 3'