Canonical Allele Identifier: CA563083214
Gene: SPRY4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1561675207
gnomAD v2: 5-141771671-CCT-C
gnomAD v3: 5-142392106-CCT-C
gnomAD v4: 5-142392106-CCT-C
MyVariant Identifiers: chr5:g.141771672_141771689delinsTCCTTCCTTCCTTCCT (hg19) chr5:g.142392107_142392124delinsTCCTTCCTTCCTTCCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.142392107_142392108del , CM000667.2:g.142392107_142392108del GRCh38
NC_000005.9:g.141771672_141771673del , CM000667.1:g.141771672_141771673del GRCh37
NC_000005.8:g.141751856_141751857del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120664.1:n.506+38524_506+38525del
Search 100 bp 5'
Search 100 bp 3'