ClinGen Allele Registry
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Canonical Allele Identifier:
CA804860503
Gene: SPRY4-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1221076026
gnomAD v3:
5-142392038-C-T
gnomAD v4:
5-142392038-C-T
MyVariant Identifiers:
chr5:g.141771603C>T (hg19)
chr5:g.142392038C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.142392038C>T , CM000667.2:g.142392038C>T
GRCh38
NC_000005.9:g.141771603C>T , CM000667.1:g.141771603C>T
GRCh37
NC_000005.8:g.141751787C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_120664.1:n.506+38455C>T
Search 100 bp 5'
Search 100 bp 3'