Canonical Allele Identifier: CA16621521
Gene: PROP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424617
ClinVar RCV Id: RCV000487438
dbSNP Id: rs1064797071

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995931C>G , CM000667.2:g.177995931C>G GRCh38
NC_000005.9:g.177422932C>G , CM000667.1:g.177422932C>G GRCh37
NC_000005.8:g.177355538C>G NCBI36
NG_015889.1:g.5312G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.3G>C MANE Select ENSP00000311290.2:p.Met1Ile
NM_006261.4:c.3G>C NP_006252.3:p.Met1Ile
NM_006261.5:c.3G>C MANE Select NP_006252.4:p.Met1Ile