Canonical Allele Identifier: CA2676773927
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992532-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992532T>A , CM000667.2:g.177992532T>A GRCh38
NC_000005.9:g.177419533T>A , CM000667.1:g.177419533T>A GRCh37
NC_000005.8:g.177352139T>A NCBI36
NG_015889.1:g.8711A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*177A>T MANE Select ENSP00000311290.2:n.*177A>T
NM_006261.4:c.*177A>T NP_006252.3:n.*177A>T
NM_006261.5:c.*177A>T MANE Select NP_006252.4:n.*177A>T
Search 100 bp 5'
Search 100 bp 3'