Canonical Allele Identifier: CA3587507
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs768922479

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992855G>T , CM000667.2:g.177992855G>T GRCh38
NC_000005.9:g.177419856G>T , CM000667.1:g.177419856G>T GRCh37
NC_000005.8:g.177352462G>T NCBI36
NG_015889.1:g.8388C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.535C>A MANE Select ENSP00000311290.2:p.Pro179Thr
NM_006261.4:c.535C>A NP_006252.3:p.Pro179Thr
NM_006261.5:c.535C>A MANE Select NP_006252.4:p.Pro179Thr