ClinGen Allele Registry
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Canonical Allele Identifier:
CA804860705
Gene: SPRY4-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1267206566
gnomAD v3:
5-142392101-T-TC
gnomAD v4:
5-142392101-T-TC
MyVariant Identifiers:
chr5:g.141771666_141771667insC (hg19)
chr5:g.142392101_142392102insC (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.142392103dup , CM000667.2:g.142392103dup
GRCh38
NC_000005.9:g.141771668dup , CM000667.1:g.141771668dup
GRCh37
NC_000005.8:g.141751852dup
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120664.1:n.506+38520dup
Search 100 bp 5'
Search 100 bp 3'