Canonical Allele Identifier: CA504967677
Gene: GIPC3 HGNC NCBI

Linked Data

dbSNP Id: rs1458681443
gnomAD v2: 19-3585718-G-T
gnomAD v4: 19-3585720-G-T
MyVariant Identifiers: chr19:g.3585718G>T (hg19) chr19:g.3585720G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3585720G>T , CM000681.2:g.3585720G>T GRCh38
NC_000019.9:g.3585718G>T , CM000681.1:g.3585718G>T GRCh37
NC_000019.8:g.3536718G>T NCBI36
NG_031943.1:g.5150G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644452.3:c.123G>T MANE Select ENSP00000493901.2:p.Thr41=
ENST00000644946.1:c.123G>T ENSP00000495068.1:p.Thr41=
ENST00000322315.5:c.123G>T ENSP00000319254.5:p.Thr41=
NM_133261.2:c.123G>T NP_573568.1:p.Thr41=
XM_005259492.2:c.123G>T XP_005259549.1:p.Thr41=
XM_005259492.3:c.123G>T XP_005259549.1:p.Thr41=
NM_133261.3:c.123G>T MANE Select NP_573568.1:p.Thr41=
Search 100 bp 5'
Search 100 bp 3'