Canonical Allele Identifier: CA564025476
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v2: 5-158755696-G-T
MyVariant Identifiers: chr5:g.158755696G>T (hg19) chr5:g.159328688G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328688G>T , CM000667.2:g.159328688G>T GRCh38
NC_000005.9:g.158755696G>T , CM000667.1:g.158755696G>T GRCh37
NC_000005.8:g.158688274G>T NCBI36
NG_009618.1:g.6786C>A , LRG_71:g.6786C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+1744C>A ENSP00000512849.1:n.-149+1744C>A
ENST00000696751.1:c.-1+1744C>A ENSP00000512850.1:n.-1+1744C>A
ENST00000696752.1:n.432+1744C>A
ENST00000231228.3:c.-1+1744C>A MANE Select ENSP00000231228.2:n.-1+1744C>A
ENST00000231228.2:c.-1+1744C>A ENSP00000231228.2:n.-1+1744C>A
NM_002187.2:c.-1+1744C>A , LRG_71t1:c.-1+1744C>A NP_002178.2:n.-1+1744C>A
NM_002187.3:c.-1+1744C>A MANE Select NP_002178.2:n.-1+1744C>A
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