Canonical Allele Identifier: CA268398641
Gene: ENTREP2 HGNC NCBI

Linked Data

dbSNP Id: rs988812888
gnomAD v3: 15-29596132-T-C
gnomAD v4: 15-29596132-T-C
MyVariant Identifiers: chr15:g.29888336T>C (hg19) chr15:g.29596132T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.29596132T>C , CM000677.2:g.29596132T>C GRCh38
NC_000015.9:g.29888336T>C , CM000677.1:g.29888336T>C GRCh37
NC_000015.8:g.27675628T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001387215.1:c.-70+78967A>G NP_001374144.1:n.-70+78967A>G
NM_001387216.1:c.-70+78967A>G NP_001374145.1:n.-70+78967A>G
NM_001387217.1:c.-70+78967A>G NP_001374146.1:n.-70+78967A>G
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