Canonical Allele Identifier: CA2680487729
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs1774090479
gnomAD v4: 6-136822518-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822518C>A , CM000668.2:g.136822518C>A GRCh38
NC_000006.11:g.137143656C>A , CM000668.1:g.137143656C>A GRCh37
NC_000006.10:g.137185349C>A NCBI36
NG_008462.1:g.4939C>A

Transcript Alleles

HGVS Amino-acid Change
XM_006715502.1:c.-148C>A XP_006715565.1:n.-148C>A
XM_011535900.1:c.-148C>A XP_011534202.1:n.-148C>A
XM_006715502.2:c.-148C>A XP_006715565.1:n.-148C>A
XM_017010934.2:c.-148C>A XP_016866423.1:n.-148C>A
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