Canonical Allele Identifier: CA1094887163
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs1774090734

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822541C>G , CM000668.2:g.136822541C>G GRCh38
NC_000006.11:g.137143679C>G , CM000668.1:g.137143679C>G GRCh37
NC_000006.10:g.137185372C>G NCBI36
NG_008462.1:g.4962C>G

Transcript Alleles

HGVS Amino-acid change
XM_006715502.1:c.-125C>G XP_006715565.1:n.-125C>G
XM_011535900.1:c.-125C>G XP_011534202.1:n.-125C>G
XM_006715502.2:c.-125C>G XP_006715565.1:n.-125C>G
XM_017010934.2:c.-125C>G XP_016866423.1:n.-125C>G