Canonical Allele Identifier: CA2676773898
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992521-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992521C>T , CM000667.2:g.177992521C>T GRCh38
NC_000005.9:g.177419522C>T , CM000667.1:g.177419522C>T GRCh37
NC_000005.8:g.177352128C>T NCBI36
NG_015889.1:g.8722G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*188G>A MANE Select ENSP00000311290.2:n.*188G>A
NM_006261.4:c.*188G>A NP_006252.3:n.*188G>A
NM_006261.5:c.*188G>A MANE Select NP_006252.4:n.*188G>A
Search 100 bp 5'
Search 100 bp 3'