Canonical Allele Identifier: CA808117149
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1278770499
gnomAD v4: 5-177992692-G-A
MyVariant Identifiers: chr5:g.177419693G>A (hg19) chr5:g.177992692G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992692G>A , CM000667.2:g.177992692G>A GRCh38
NC_000005.9:g.177419693G>A , CM000667.1:g.177419693G>A GRCh37
NC_000005.8:g.177352299G>A NCBI36
NG_015889.1:g.8551C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*17C>T MANE Select ENSP00000311290.2:n.*17C>T
NM_006261.4:c.*17C>T NP_006252.3:n.*17C>T
NM_006261.5:c.*17C>T MANE Select NP_006252.4:n.*17C>T
Search 100 bp 5'
Search 100 bp 3'