Canonical Allele Identifier: CA132897457
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs771543956
gnomAD v3: 5-177993114-A-T
gnomAD v4: 5-177993114-A-T
MyVariant Identifiers: chr5:g.177420115A>T (hg19) chr5:g.177993114A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993114A>T , CM000667.2:g.177993114A>T GRCh38
NC_000005.9:g.177420115A>T , CM000667.1:g.177420115A>T GRCh37
NC_000005.8:g.177352721A>T NCBI36
NG_015889.1:g.8129T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-67T>A MANE Select ENSP00000311290.2:n.343-67T>A
NM_006261.4:c.343-67T>A NP_006252.3:n.343-67T>A
NM_006261.5:c.343-67T>A MANE Select NP_006252.4:n.343-67T>A
Search 100 bp 5'
Search 100 bp 3'