Canonical Allele Identifier: CA836257805
Gene:

Linked Data

dbSNP Id: rs1184575084
MyVariant Identifiers: chr7:g.17997584G>C (hg19) chr7:g.17957961G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957961G>C , CM000669.2:g.17957961G>C GRCh38
NC_000007.13:g.17997584G>C , CM000669.1:g.17997584G>C GRCh37
NC_000007.12:g.17964109G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-709G>C
Search 100 bp 5'
Search 100 bp 3'