Canonical Allele Identifier: CA350637823

Gene: IHH

Linked Data

• gnomAD v4: 2-219060461-G-T
• MyVariant Identifiers: chr2:g.219925183G>T (hg19) ; chr2:g.219060461G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219060461G>T , CM000664.2:g.219060461G>T	GRCh38
NC_000002.11:g.219925183G>T , CM000664.1:g.219925183G>T	GRCh37
NC_000002.10:g.219633427G>T	NCBI36
NG_016741.1:g.5056C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295731.7:c.7C>A MANE Select	ENSP00000295731.5:p.Pro3Thr
ENST00000295731.6:c.7C>A	ENSP00000295731.5:p.Pro3Thr
NM_002181.3:c.7C>A	NP_002172.2:p.Pro3Thr
NM_002181.4:c.7C>A MANE Select	NP_002172.2:p.Pro3Thr