Canonical Allele Identifier: CA362379446
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177995842-G-A
MyVariant Identifiers: chr5:g.177422843G>A (hg19) chr5:g.177995842G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995842G>A , CM000667.2:g.177995842G>A GRCh38
NC_000005.9:g.177422843G>A , CM000667.1:g.177422843G>A GRCh37
NC_000005.8:g.177355449G>A NCBI36
NG_015889.1:g.5401C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.92C>T MANE Select ENSP00000311290.2:p.Thr31Ile
NM_006261.4:c.92C>T NP_006252.3:p.Thr31Ile
NM_006261.5:c.92C>T MANE Select NP_006252.4:p.Thr31Ile
Search 100 bp 5'
Search 100 bp 3'