Canonical Allele Identifier: CA132896942
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs919089967
gnomAD v3: 5-177992599-C-A
gnomAD v4: 5-177992599-C-A
MyVariant Identifiers: chr5:g.177419600C>A (hg19) chr5:g.177992599C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992599C>A , CM000667.2:g.177992599C>A GRCh38
NC_000005.9:g.177419600C>A , CM000667.1:g.177419600C>A GRCh37
NC_000005.8:g.177352206C>A NCBI36
NG_015889.1:g.8644G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*110G>T MANE Select ENSP00000311290.2:n.*110G>T
NM_006261.4:c.*110G>T NP_006252.3:n.*110G>T
NM_006261.5:c.*110G>T MANE Select NP_006252.4:n.*110G>T
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