Canonical Allele Identifier: CA362032697
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320407-C-T
MyVariant Identifiers: chr5:g.158747415C>T (hg19) chr5:g.159320407C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320407C>T , CM000667.2:g.159320407C>T GRCh38
NC_000005.9:g.158747415C>T , CM000667.1:g.158747415C>T GRCh37
NC_000005.8:g.158679993C>T NCBI36
NG_009618.1:g.15067G>A , LRG_71:g.15067G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-35G>A ENSP00000512849.1:n.-35G>A
ENST00000696751.1:c.*91G>A ENSP00000512850.1:n.*91G>A
ENST00000231228.3:c.596G>A MANE Select ENSP00000231228.2:p.Cys199Tyr
ENST00000231228.2:c.596G>A ENSP00000231228.2:p.Cys199Tyr
NM_002187.2:c.596G>A , LRG_71t1:c.596G>A NP_002178.2:p.Cys199Tyr
NM_002187.3:c.596G>A MANE Select NP_002178.2:p.Cys199Tyr
Search 100 bp 5'
Search 100 bp 3'