Canonical Allele Identifier: CA448355243
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1167319896
gnomAD v3: 5-177992970-A-G
gnomAD v4: 5-177992970-A-G
MyVariant Identifiers: chr5:g.177419971A>G (hg19) chr5:g.177992970A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992970A>G , CM000667.2:g.177992970A>G GRCh38
NC_000005.9:g.177419971A>G , CM000667.1:g.177419971A>G GRCh37
NC_000005.8:g.177352577A>G NCBI36
NG_015889.1:g.8273T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.420T>C MANE Select ENSP00000311290.2:p.Pro140=
NM_006261.4:c.420T>C NP_006252.3:p.Pro140=
NM_006261.5:c.420T>C MANE Select NP_006252.4:p.Pro140=
Search 100 bp 5'
Search 100 bp 3'