ClinGen Allele Registry
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Canonical Allele Identifier:
CA128897585
Gene: SPRY4-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs561216043
gnomAD v2:
5-141771733-T-C
gnomAD v3:
5-142392168-T-C
gnomAD v4:
5-142392168-T-C
MyVariant Identifiers:
chr5:g.141771733T>C (hg19)
chr5:g.142392168T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.142392168T>C , CM000667.2:g.142392168T>C
GRCh38
NC_000005.9:g.141771733T>C , CM000667.1:g.141771733T>C
GRCh37
NC_000005.8:g.141751917T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120664.1:n.506+38585T>C
Search 100 bp 5'
Search 100 bp 3'