Canonical Allele Identifier: CA2676773913
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992528-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992528T>A , CM000667.2:g.177992528T>A GRCh38
NC_000005.9:g.177419529T>A , CM000667.1:g.177419529T>A GRCh37
NC_000005.8:g.177352135T>A NCBI36
NG_015889.1:g.8715A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*181A>T MANE Select ENSP00000311290.2:n.*181A>T
NM_006261.4:c.*181A>T NP_006252.3:n.*181A>T
NM_006261.5:c.*181A>T MANE Select NP_006252.4:n.*181A>T
Search 100 bp 5'
Search 100 bp 3'