Canonical Allele Identifier: CA132896963

Gene: PROP1

Linked Data

• dbSNP Id: rs1048977006
• MyVariant Identifiers: chr5:g.177419645C>G (hg19) ; chr5:g.177992644C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177992644C>G , CM000667.2:g.177992644C>G	GRCh38
NC_000005.9:g.177419645C>G , CM000667.1:g.177419645C>G	GRCh37
NC_000005.8:g.177352251C>G	NCBI36
NG_015889.1:g.8599G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.*65G>C MANE Select	ENSP00000311290.2:n.*65G>C
NM_006261.4:c.*65G>C	NP_006252.3:n.*65G>C
NM_006261.5:c.*65G>C MANE Select	NP_006252.4:n.*65G>C