Canonical Allele Identifier: CA819499561
Gene: PEX7 HGNC NCBI

Linked Data

dbSNP Id: rs1197328398

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822527A>G , CM000668.2:g.136822527A>G GRCh38
NC_000006.11:g.137143665A>G , CM000668.1:g.137143665A>G GRCh37
NC_000006.10:g.137185358A>G NCBI36
NG_008462.1:g.4948A>G

Transcript Alleles

HGVS Amino-acid change
XM_006715502.1:c.-139A>G XP_006715565.1:n.-139A>G
XM_011535900.1:c.-139A>G XP_011534202.1:n.-139A>G
XM_006715502.2:c.-139A>G XP_006715565.1:n.-139A>G
XM_017010934.2:c.-139A>G XP_016866423.1:n.-139A>G