Canonical Allele Identifier: CA2676774171
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992634-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992634A>G , CM000667.2:g.177992634A>G GRCh38
NC_000005.9:g.177419635A>G , CM000667.1:g.177419635A>G GRCh37
NC_000005.8:g.177352241A>G NCBI36
NG_015889.1:g.8609T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*75T>C MANE Select ENSP00000311290.2:n.*75T>C
NM_006261.4:c.*75T>C NP_006252.3:n.*75T>C
NM_006261.5:c.*75T>C MANE Select NP_006252.4:n.*75T>C
Search 100 bp 5'
Search 100 bp 3'