Canonical Allele Identifier: CA819499558
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs1375452745

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822526G>A , CM000668.2:g.136822526G>A GRCh38
NC_000006.11:g.137143664G>A , CM000668.1:g.137143664G>A GRCh37
NC_000006.10:g.137185357G>A NCBI36
NG_008462.1:g.4947G>A

Transcript Alleles

HGVS Amino-acid change
XM_006715502.1:c.-140G>A XP_006715565.1:n.-140G>A
XM_011535900.1:c.-140G>A XP_011534202.1:n.-140G>A
XM_006715502.2:c.-140G>A XP_006715565.1:n.-140G>A
XM_017010934.2:c.-140G>A XP_016866423.1:n.-140G>A