Canonical Allele Identifier: CA564025324
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1381556892
gnomAD v2: 5-158754507-A-G
gnomAD v3: 5-159327499-A-G
gnomAD v4: 5-159327499-A-G
MyVariant Identifiers: chr5:g.158754507A>G (hg19) chr5:g.159327499A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327499A>G , CM000667.2:g.159327499A>G GRCh38
NC_000005.9:g.158754507A>G , CM000667.1:g.158754507A>G GRCh37
NC_000005.8:g.158687085A>G NCBI36
NG_009618.1:g.7975T>C , LRG_71:g.7975T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+2933T>C ENSP00000512849.1:n.-149+2933T>C
ENST00000696751.1:c.1-717T>C ENSP00000512850.1:n.1-717T>C
ENST00000696752.1:n.433-717T>C
ENST00000231228.3:c.1-717T>C MANE Select ENSP00000231228.2:n.1-717T>C
ENST00000231228.2:c.1-717T>C ENSP00000231228.2:n.1-717T>C
NM_002187.2:c.1-717T>C , LRG_71t1:c.1-717T>C NP_002178.2:n.1-717T>C
NM_002187.3:c.1-717T>C MANE Select NP_002178.2:n.1-717T>C
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