Canonical Allele Identifier: CA2680487759
Gene: PEX7 HGNC NCBI

Linked Data

gnomAD v4: 6-136822540-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822540T>C , CM000668.2:g.136822540T>C GRCh38
NC_000006.11:g.137143678T>C , CM000668.1:g.137143678T>C GRCh37
NC_000006.10:g.137185371T>C NCBI36
NG_008462.1:g.4961T>C

Transcript Alleles

HGVS Amino-acid change
XM_006715502.1:c.-126T>C XP_006715565.1:n.-126T>C
XM_011535900.1:c.-126T>C XP_011534202.1:n.-126T>C
XM_006715502.2:c.-126T>C XP_006715565.1:n.-126T>C
XM_017010934.2:c.-126T>C XP_016866423.1:n.-126T>C
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