Canonical Allele Identifier: CA2676774181
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992640-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992640C>A , CM000667.2:g.177992640C>A GRCh38
NC_000005.9:g.177419641C>A , CM000667.1:g.177419641C>A GRCh37
NC_000005.8:g.177352247C>A NCBI36
NG_015889.1:g.8603G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*69G>T MANE Select ENSP00000311290.2:n.*69G>T
NM_006261.4:c.*69G>T NP_006252.3:n.*69G>T
NM_006261.5:c.*69G>T MANE Select NP_006252.4:n.*69G>T
Search 100 bp 5'
Search 100 bp 3'