Canonical Allele Identifier: CA350637737

Gene: IHH

Linked Data

• MyVariant Identifiers: chr2:g.219925156A>G (hg19) ; chr2:g.219060434A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219060434A>G , CM000664.2:g.219060434A>G	GRCh38
NC_000002.11:g.219925156A>G , CM000664.1:g.219925156A>G	GRCh37
NC_000002.10:g.219633400A>G	NCBI36
NG_016741.1:g.5083T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295731.7:c.34T>C MANE Select	ENSP00000295731.5:p.Phe12Leu
ENST00000295731.6:c.34T>C	ENSP00000295731.5:p.Phe12Leu
NM_002181.3:c.34T>C	NP_002172.2:p.Phe12Leu
NM_002181.4:c.34T>C MANE Select	NP_002172.2:p.Phe12Leu