Canonical Allele Identifier: CA15779807
Gene: MIPEP HGNC NCBI

Linked Data

dbSNP Id: rs9318086
gnomAD v2: 13-24432467-A-G
gnomAD v3: 13-23858328-A-G
gnomAD v4: 13-23858328-A-G
MyVariant Identifiers: chr13:g.24432467A>G (hg19) chr13:g.23858328A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23858328A>G , CM000675.2:g.23858328A>G GRCh38
NC_000013.10:g.24432467A>G , CM000675.1:g.24432467A>G GRCh37
NC_000013.9:g.23330467A>G NCBI36
NG_052977.1:g.36121T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382172.4:c.1106+532T>C MANE Select ENSP00000371607.3:n.1106+532T>C
ENST00000382172.3:c.1106+532T>C ENSP00000371607.3:n.1106+532T>C
ENST00000494139.1:n.503+532T>C
NM_005932.3:c.1106+532T>C NP_005923.2:n.1106+532T>C
XM_011535097.1:c.920+532T>C XP_011533399.1:n.920+532T>C
XM_011535098.1:c.1106+532T>C XP_011533400.1:n.1106+532T>C
XM_011535097.2:c.920+532T>C XP_011533399.1:n.920+532T>C
XM_011535098.3:c.1106+532T>C XP_011533400.1:n.1106+532T>C
NM_005932.4:c.1106+532T>C MANE Select NP_005923.3:n.1106+532T>C
Search 100 bp 5'
Search 100 bp 3'