ClinGen Allele Registry
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Canonical Allele Identifier:
CA128897569
Gene: SPRY4-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs868018784
gnomAD v2:
5-141771697-T-C
gnomAD v3:
5-142392132-T-C
gnomAD v4:
5-142392132-T-C
MyVariant Identifiers:
chr5:g.141771697T>C (hg19)
chr5:g.141771697_141771723delinsCTCCTTCCTTCCTTCCTTCCTTCCTTC (hg19)
chr5:g.142392132T>C (hg38)
chr5:g.142392132_142392158delinsCTCCTTCCTTCCTTCCTTCCTTCCTTC (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.142392132T>C , CM000667.2:g.142392132T>C
GRCh38
NC_000005.9:g.141771697T>C , CM000667.1:g.141771697T>C
GRCh37
NC_000005.8:g.141751881T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120664.1:n.506+38549T>C
Search 100 bp 5'
Search 100 bp 3'