Canonical Allele Identifier: CA2663194941
Gene: IHH HGNC NCBI

Linked Data

gnomAD v4: 2-219060071-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060071G>T , CM000664.2:g.219060071G>T GRCh38
NC_000002.11:g.219924793G>T , CM000664.1:g.219924793G>T GRCh37
NC_000002.10:g.219633037G>T NCBI36
NG_016741.1:g.5446C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.315+82C>A MANE Select ENSP00000295731.5:n.315+82C>A
ENST00000295731.6:c.315+82C>A ENSP00000295731.5:n.315+82C>A
NM_002181.3:c.315+82C>A NP_002172.2:n.315+82C>A
NM_002181.4:c.315+82C>A MANE Select NP_002172.2:n.315+82C>A
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