Canonical Allele Identifier: CA1329042631
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060299G= , CM000664.2:g.219060299G= GRCh38
NC_000002.11:g.219925021G= , CM000664.1:g.219925021G= GRCh37
NC_000002.10:g.219633265G= NCBI36
NG_016741.1:g.5218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.169C= MANE Select ENSP00000295731.5:p.Pro57=
ENST00000295731.6:c.169C= ENSP00000295731.5:p.Pro57=
NM_002181.3:c.169C= NP_002172.2:p.Pro57=
NM_002181.4:c.169C= MANE Select NP_002172.2:p.Pro57=
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