Canonical Allele Identifier: CA3587566
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2975798
ClinVar RCV Id: RCV003833884
dbSNP Id: rs760209079
ExAC: 5:177421164 G / A
gnomAD v2: 5-177421164-G-A
gnomAD v3: 5-177994163-G-A
gnomAD v4: 5-177994163-G-A
MyVariant Identifiers: chr5:g.177421164G>A (hg19) chr5:g.177994163G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177994163G>A , CM000667.2:g.177994163G>A GRCh38
NC_000005.9:g.177421164G>A , CM000667.1:g.177421164G>A GRCh37
NC_000005.8:g.177353770G>A NCBI36
NG_015889.1:g.7080C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.285C>T MANE Select ENSP00000311290.2:p.Asp95=
NM_006261.4:c.285C>T NP_006252.3:p.Asp95=
NM_006261.5:c.285C>T MANE Select NP_006252.4:p.Asp95=
Search 100 bp 5'
Search 100 bp 3'