Canonical Allele Identifier: CA2680487770
Gene: PEX7 HGNC NCBI

Linked Data

gnomAD v4: 6-136822546-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.136822546A>T , CM000668.2:g.136822546A>T GRCh38
NC_000006.11:g.137143684A>T , CM000668.1:g.137143684A>T GRCh37
NC_000006.10:g.137185377A>T NCBI36
NG_008462.1:g.4967A>T

Transcript Alleles

HGVS Amino-acid change
XM_006715502.1:c.-120A>T XP_006715565.1:n.-120A>T
XM_011535900.1:c.-120A>T XP_011534202.1:n.-120A>T
XM_006715502.2:c.-120A>T XP_006715565.1:n.-120A>T
XM_017010934.2:c.-120A>T XP_016866423.1:n.-120A>T
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