Canonical Allele Identifier: CA41486669
Gene:

Linked Data

dbSNP Id: rs138192038
MyVariant Identifiers: chr2:g.632792_632793insGTT (hg19) chr2:g.632792_632793insGTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.632792_632793insGTT , CM000664.2:g.632792_632793insGTT GRCh38
NC_000002.11:g.632792_632793insGTT , CM000664.1:g.632792_632793insGTT GRCh37
NC_000002.10:g.622792_622793insGTT NCBI36
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