Canonical Allele Identifier: CA431419640
Gene: IHH HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219925118C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060396C>A , CM000664.2:g.219060396C>A GRCh38
NC_000002.11:g.219925118C>A , CM000664.1:g.219925118C>A GRCh37
NC_000002.10:g.219633362C>A NCBI36
NG_016741.1:g.5121G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.72G>T MANE Select ENSP00000295731.5:p.Ala24=
ENST00000295731.6:c.72G>T ENSP00000295731.5:p.Ala24=
NM_002181.3:c.72G>T NP_002172.2:p.Ala24=
NM_002181.4:c.72G>T MANE Select NP_002172.2:p.Ala24=