Canonical Allele Identifier: CA431419527
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925088C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060366C>G , CM000664.2:g.219060366C>G GRCh38
NC_000002.11:g.219925088C>G , CM000664.1:g.219925088C>G GRCh37
NC_000002.10:g.219633332C>G NCBI36
NG_016741.1:g.5151G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.102G>C MANE Select ENSP00000295731.5:p.Val34=
ENST00000295731.6:c.102G>C ENSP00000295731.5:p.Val34=
NM_002181.3:c.102G>C NP_002172.2:p.Val34=
NM_002181.4:c.102G>C MANE Select NP_002172.2:p.Val34=
Search 100 bp 5'
Search 100 bp 3'