Canonical Allele Identifier: CA2680487635
Gene: PEX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822461A>G , CM000668.2:g.136822461A>G GRCh38
NC_000006.11:g.137143599A>G , CM000668.1:g.137143599A>G GRCh37
NC_000006.10:g.137185292A>G NCBI36
NG_008462.1:g.4882A>G

Transcript Alleles

HGVS Amino-acid Change
XM_006715502.1:c.-205A>G XP_006715565.1:n.-205A>G
XM_011535900.1:c.-205A>G XP_011534202.1:n.-205A>G
XM_006715502.2:c.-205A>G XP_006715565.1:n.-205A>G
XM_017010934.2:c.-205A>G XP_016866423.1:n.-205A>G