Canonical Allele Identifier: CA2676773962
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992547-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992547A>C , CM000667.2:g.177992547A>C GRCh38
NC_000005.9:g.177419548A>C , CM000667.1:g.177419548A>C GRCh37
NC_000005.8:g.177352154A>C NCBI36
NG_015889.1:g.8696T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*162T>G MANE Select ENSP00000311290.2:n.*162T>G
NM_006261.4:c.*162T>G NP_006252.3:n.*162T>G
NM_006261.5:c.*162T>G MANE Select NP_006252.4:n.*162T>G
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