Canonical Allele Identifier: CA350636743
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219924917G>C (hg19) chr2:g.219060195G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060195G>C , CM000664.2:g.219060195G>C GRCh38
NC_000002.11:g.219924917G>C , CM000664.1:g.219924917G>C GRCh37
NC_000002.10:g.219633161G>C NCBI36
NG_016741.1:g.5322C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.273C>G MANE Select ENSP00000295731.5:p.Phe91Leu
ENST00000295731.6:c.273C>G ENSP00000295731.5:p.Phe91Leu
NM_002181.3:c.273C>G NP_002172.2:p.Phe91Leu
NM_002181.4:c.273C>G MANE Select NP_002172.2:p.Phe91Leu
Search 100 bp 5'
Search 100 bp 3'