Canonical Allele Identifier: CA808117856

Gene: PROP1

Linked Data

• dbSNP Id: rs1214256480
• MyVariant Identifiers: chr5:g.177420058G>A (hg19) ; chr5:g.177993057G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177993057G>A , CM000667.2:g.177993057G>A	GRCh38
NC_000005.9:g.177420058G>A , CM000667.1:g.177420058G>A	GRCh37
NC_000005.8:g.177352664G>A	NCBI36
NG_015889.1:g.8186C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308304.2:c.343-10C>T MANE Select	ENSP00000311290.2:n.343-10C>T
NM_006261.4:c.343-10C>T	NP_006252.3:n.343-10C>T
NM_006261.5:c.343-10C>T MANE Select	NP_006252.4:n.343-10C>T