Canonical Allele Identifier: CA132897240

Gene: PROP1

Linked Data

• dbSNP Id: rs199587578
• MyVariant Identifiers: chr5:g.177419891A>G (hg19) ; chr5:g.177992890A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992890A>G , CM000667.2:g.177992890A>G	GRCh38
NC_000005.9:g.177419891A>G , CM000667.1:g.177419891A>G	GRCh37
NC_000005.8:g.177352497A>G	NCBI36
NG_015889.1:g.8353T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.500T>C MANE Select	ENSP00000311290.2:p.Phe167Ser
NM_006261.4:c.500T>C	NP_006252.3:p.Phe167Ser
NM_006261.5:c.500T>C MANE Select	NP_006252.4:p.Phe167Ser