Canonical Allele Identifier: CA129831424
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs960652715
MyVariant Identifiers: chr5:g.158754064_158754065insT (hg19) chr5:g.159327056_159327057insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327056_159327057insT , CM000667.2:g.159327056_159327057insT GRCh38
NC_000005.9:g.158754064_158754065insT , CM000667.1:g.158754064_158754065insT GRCh37
NC_000005.8:g.158686642_158686643insT NCBI36
NG_009618.1:g.8417_8418insA , LRG_71:g.8417_8418insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+3375_-149+3376insA ENSP00000512849.1:n.-149+3375_-149+3376insA
ENST00000696751.1:c.1-275_1-274insA ENSP00000512850.1:n.1-275_1-274insA
ENST00000696752.1:n.433-275_433-274insA
ENST00000231228.3:c.1-275_1-274insA MANE Select ENSP00000231228.2:n.1-275_1-274insA
ENST00000231228.2:c.1-275_1-274insA ENSP00000231228.2:n.1-275_1-274insA
NM_002187.2:c.1-275_1-274insA , LRG_71t1:c.1-275_1-274insA NP_002178.2:n.1-275_1-274insA
NM_002187.3:c.1-275_1-274insA MANE Select NP_002178.2:n.1-275_1-274insA
Search 100 bp 5'
Search 100 bp 3'