Canonical Allele Identifier: CA426411720
Gene: PEX13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.61259067A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61031932A>G , CM000664.2:g.61031932A>G GRCh38
NC_000002.11:g.61259067A>G , CM000664.1:g.61259067A>G GRCh37
NC_000002.10:g.61112571A>G NCBI36
NG_008665.1:g.19256A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295030.6:c.606A>G MANE Select ENSP00000295030.4:p.Arg202=
ENST00000295030.5:c.606A>G ENSP00000295030.4:p.Arg202=
NM_002618.3:c.606A>G NP_002609.1:p.Arg202=
XM_011532904.1:c.489A>G XP_011531206.1:p.Arg163=
NM_002618.4:c.606A>G MANE Select NP_002609.1:p.Arg202=
Search 100 bp 5'
Search 100 bp 3'