Canonical Allele Identifier: CA804860412
Gene: SPRY4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1191190030
MyVariant Identifiers: chr5:g.141771449C>G (hg19) chr5:g.142391884C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.142391884C>G , CM000667.2:g.142391884C>G GRCh38
NC_000005.9:g.141771449C>G , CM000667.1:g.141771449C>G GRCh37
NC_000005.8:g.141751633C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120664.1:n.506+38301C>G
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