Canonical Allele Identifier: CA613317330
Gene: IL25 HGNC NCBI

Linked Data

dbSNP Id: rs1177466024
gnomAD v2: 14-23844781-CCT-C
gnomAD v3: 14-23375572-CCT-C
gnomAD v4: 14-23375572-CCT-C
MyVariant Identifiers: chr14:g.23844782_23844783del (hg19) chr14:g.23375573_23375574del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23375577_23375578del , CM000676.2:g.23375577_23375578del GRCh38
NC_000014.8:g.23844786_23844787del , CM000676.1:g.23844786_23844787del GRCh37
NC_000014.7:g.22914626_22914627del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397242.3:c.231-48_231-47del MANE Select ENSP00000380417.2:n.231-48_231-47del
ENST00000329715.2:c.279-48_279-47del ENSP00000328111.2:n.279-48_279-47del
ENST00000397242.2:c.231-48_231-47del ENSP00000380417.2:n.231-48_231-47del
NM_022789.3:c.279-48_279-47del NP_073626.1:n.279-48_279-47del
NM_172314.1:c.231-48_231-47del NP_758525.1:n.231-48_231-47del
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