Canonical Allele Identifier: CA350636738
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219924916T>A (hg19) chr2:g.219060194T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060194T>A , CM000664.2:g.219060194T>A GRCh38
NC_000002.11:g.219924916T>A , CM000664.1:g.219924916T>A GRCh37
NC_000002.10:g.219633160T>A NCBI36
NG_016741.1:g.5323A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.274A>T MANE Select ENSP00000295731.5:p.Lys92Ter
ENST00000295731.6:c.274A>T ENSP00000295731.5:p.Lys92Ter
NM_002181.3:c.274A>T NP_002172.2:p.Lys92Ter
NM_002181.4:c.274A>T MANE Select NP_002172.2:p.Lys92Ter
Search 100 bp 5'
Search 100 bp 3'