Canonical Allele Identifier: CA362378698
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177419940T>G (hg19) chr5:g.177992939T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992939T>G , CM000667.2:g.177992939T>G GRCh38
NC_000005.9:g.177419940T>G , CM000667.1:g.177419940T>G GRCh37
NC_000005.8:g.177352546T>G NCBI36
NG_015889.1:g.8304A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.451A>C MANE Select ENSP00000311290.2:p.Thr151Pro
NM_006261.4:c.451A>C NP_006252.3:p.Thr151Pro
NM_006261.5:c.451A>C MANE Select NP_006252.4:p.Thr151Pro
Search 100 bp 5'
Search 100 bp 3'