Canonical Allele Identifier: CA711820898

Gene: ENTREP2

Linked Data

• dbSNP Id: rs1316084702
• gnomAD v3: 15-29132587-A-G
• gnomAD v4: 15-29132587-A-G
• MyVariant Identifiers: chr15:g.29424790A>G (hg19) ; chr15:g.29132587A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132587A>G , CM000677.2:g.29132587A>G	GRCh38
NC_000015.9:g.29424790A>G , CM000677.1:g.29424790A>G	GRCh37
NC_000015.8:g.27212082A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261275.5:c.928-3723T>C MANE Select	ENSP00000261275.4:n.928-3723T>C
ENST00000261275.4:c.928-3723T>C	ENSP00000261275.4:n.928-3723T>C
ENST00000560021.1:n.664-3723T>C
NM_015307.1:c.928-3723T>C	NP_056122.1:n.928-3723T>C
XM_011521407.1:c.1039-3723T>C	XP_011519709.1:n.1039-3723T>C
XM_011521407.2:c.1039-3723T>C	XP_011519709.1:n.1039-3723T>C
NM_001387214.1:c.793-3723T>C	NP_001374143.1:n.793-3723T>C
NM_001387215.1:c.640-3723T>C	NP_001374144.1:n.640-3723T>C
NM_001387216.1:c.640-3723T>C	NP_001374145.1:n.640-3723T>C
NM_001387217.1:c.505-3723T>C	NP_001374146.1:n.505-3723T>C
NM_015307.2:c.928-3723T>C MANE Select	NP_056122.1:n.928-3723T>C