Canonical Allele Identifier: CA3587641
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1138402
ClinVar RCV Id: RCV001474761
dbSNP Id: rs758032539
ExAC: 5:177422842 G / A
gnomAD v4: 5-177995841-G-A
MyVariant Identifiers: chr5:g.177422842G>A (hg19) chr5:g.177995841G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995841G>A , CM000667.2:g.177995841G>A GRCh38
NC_000005.9:g.177422842G>A , CM000667.1:g.177422842G>A GRCh37
NC_000005.8:g.177355448G>A NCBI36
NG_015889.1:g.5402C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.93C>T MANE Select ENSP00000311290.2:p.Thr31=
NM_006261.4:c.93C>T NP_006252.3:p.Thr31=
NM_006261.5:c.93C>T MANE Select NP_006252.4:p.Thr31=
Search 100 bp 5'
Search 100 bp 3'