Canonical Allele Identifier: CA447992895
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs758032539
gnomAD v3: 5-177995841-G-T
gnomAD v4: 5-177995841-G-T
MyVariant Identifiers: chr5:g.177422842G>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.93C>A MANE Select ENSP00000311290.2:p.Thr31=
NM_006261.4:c.93C>A NP_006252.3:p.Thr31=
NM_006261.5:c.93C>A MANE Select NP_006252.4:p.Thr31=
Search 100 bp 5'
Search 100 bp 3'