Canonical Allele Identifier: CA3587469
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs753674298
ExAC: 5:177419665 C / T
gnomAD v2: 5-177419665-C-T
gnomAD v4: 5-177992664-C-T
MyVariant Identifiers: chr5:g.177419665C>T (hg19) chr5:g.177992664C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992664C>T , CM000667.2:g.177992664C>T GRCh38
NC_000005.9:g.177419665C>T , CM000667.1:g.177419665C>T GRCh37
NC_000005.8:g.177352271C>T NCBI36
NG_015889.1:g.8579G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*45G>A MANE Select ENSP00000311290.2:n.*45G>A
NM_006261.4:c.*45G>A NP_006252.3:n.*45G>A
NM_006261.5:c.*45G>A MANE Select NP_006252.4:n.*45G>A
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