Canonical Allele Identifier: CA65950986
Gene: IHH HGNC NCBI

Linked Data

dbSNP Id: rs571583626
gnomAD v2: 2-219924802-C-A
gnomAD v3: 2-219060080-C-A
gnomAD v4: 2-219060080-C-A
MyVariant Identifiers: chr2:g.219924802C>A (hg19) chr2:g.219060080C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060080C>A , CM000664.2:g.219060080C>A GRCh38
NC_000002.11:g.219924802C>A , CM000664.1:g.219924802C>A GRCh37
NC_000002.10:g.219633046C>A NCBI36
NG_016741.1:g.5437G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295731.7:c.315+73G>T MANE Select ENSP00000295731.5:n.315+73G>T
ENST00000295731.6:c.315+73G>T ENSP00000295731.5:n.315+73G>T
NM_002181.3:c.315+73G>T NP_002172.2:n.315+73G>T
NM_002181.4:c.315+73G>T MANE Select NP_002172.2:n.315+73G>T
Search 100 bp 5'
Search 100 bp 3'