Canonical Allele Identifier: CA2680487709
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs930411628

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822502G>T , CM000668.2:g.136822502G>T GRCh38
NC_000006.11:g.137143640G>T , CM000668.1:g.137143640G>T GRCh37
NC_000006.10:g.137185333G>T NCBI36
NG_008462.1:g.4923G>T

Transcript Alleles

HGVS Amino-acid Change
XM_006715502.1:c.-164G>T XP_006715565.1:n.-164G>T
XM_011535900.1:c.-164G>T XP_011534202.1:n.-164G>T
XM_006715502.2:c.-164G>T XP_006715565.1:n.-164G>T
XM_017010934.2:c.-164G>T XP_016866423.1:n.-164G>T