Canonical Allele Identifier: CA563083176
Gene: SPRY4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1561675101
gnomAD v2: 5-141771645-CTCCTTCCTTCCCTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT-C
gnomAD v3: 5-142392080-CTCCTTCCTTCCCTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT-C
gnomAD v4: 5-142392080-CTCCTTCCTTCCCTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT-C
MyVariant Identifiers: chr5:g.141771646_141771689del (hg19) chr5:g.142392081_142392124del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.142392092_142392135del , CM000667.2:g.142392092_142392135del GRCh38
NC_000005.9:g.141771657_141771700del , CM000667.1:g.141771657_141771700del GRCh37
NC_000005.8:g.141751841_141751884del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120664.1:n.506+38509_506+38552del
Search 100 bp 5'
Search 100 bp 3'