Canonical Allele Identifier: CA431419864
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060192-C-T
MyVariant Identifiers: chr2:g.219924914C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060192C>T , CM000664.2:g.219060192C>T GRCh38
NC_000002.11:g.219924914C>T , CM000664.1:g.219924914C>T GRCh37
NC_000002.10:g.219633158C>T NCBI36
NG_016741.1:g.5325G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.276G>A MANE Select ENSP00000295731.5:p.Lys92=
ENST00000295731.6:c.276G>A ENSP00000295731.5:p.Lys92=
NM_002181.3:c.276G>A NP_002172.2:p.Lys92=
NM_002181.4:c.276G>A MANE Select NP_002172.2:p.Lys92=
Search 100 bp 5'
Search 100 bp 3'