Canonical Allele Identifier: CA711861569
Gene: ENTREP2 HGNC NCBI

Linked Data

dbSNP Id: rs1175673568

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.29596100T>C , CM000677.2:g.29596100T>C GRCh38
NC_000015.9:g.29888304T>C , CM000677.1:g.29888304T>C GRCh37
NC_000015.8:g.27675596T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001387215.1:c.-70+78999A>G NP_001374144.1:n.-70+78999A>G
NM_001387216.1:c.-70+78999A>G NP_001374145.1:n.-70+78999A>G
NM_001387217.1:c.-70+78999A>G NP_001374146.1:n.-70+78999A>G