Canonical Allele Identifier: CA362379436
Gene: PROP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.177422837G>C (hg19) chr5:g.177995836G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177995836G>C , CM000667.2:g.177995836G>C GRCh38
NC_000005.9:g.177422837G>C , CM000667.1:g.177422837G>C GRCh37
NC_000005.8:g.177355443G>C NCBI36
NG_015889.1:g.5407C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308304.2:c.98C>G MANE Select ENSP00000311290.2:p.Thr33Ser
NM_006261.4:c.98C>G NP_006252.3:p.Thr33Ser
NM_006261.5:c.98C>G MANE Select NP_006252.4:p.Thr33Ser
Search 100 bp 5'
Search 100 bp 3'