Canonical Allele Identifier: CA132899297
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs903475583
gnomAD v2: 5-177422837-G-T
gnomAD v4: 5-177995836-G-T
MyVariant Identifiers: chr5:g.177422837G>T (hg19) chr5:g.177995836G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995836G>T , CM000667.2:g.177995836G>T GRCh38
NC_000005.9:g.177422837G>T , CM000667.1:g.177422837G>T GRCh37
NC_000005.8:g.177355443G>T NCBI36
NG_015889.1:g.5407C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.98C>A MANE Select ENSP00000311290.2:p.Thr33Asn
NM_006261.4:c.98C>A NP_006252.3:p.Thr33Asn
NM_006261.5:c.98C>A MANE Select NP_006252.4:p.Thr33Asn
Search 100 bp 5'
Search 100 bp 3'