Canonical Allele Identifier: CA968120638

Gene: ENTREP2

Linked Data

• dbSNP Id: rs2045693902
• gnomAD v3: 15-29132566-C-A
• gnomAD v4: 15-29132566-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132566C>A , CM000677.2:g.29132566C>A	GRCh38
NC_000015.9:g.29424769C>A , CM000677.1:g.29424769C>A	GRCh37
NC_000015.8:g.27212061C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261275.5:c.928-3702G>T MANE Select	ENSP00000261275.4:n.928-3702G>T
ENST00000261275.4:c.928-3702G>T	ENSP00000261275.4:n.928-3702G>T
ENST00000560021.1:n.664-3702G>T
NM_015307.1:c.928-3702G>T	NP_056122.1:n.928-3702G>T
XM_011521407.1:c.1039-3702G>T	XP_011519709.1:n.1039-3702G>T
XM_011521407.2:c.1039-3702G>T	XP_011519709.1:n.1039-3702G>T
NM_001387214.1:c.793-3702G>T	NP_001374143.1:n.793-3702G>T
NM_001387215.1:c.640-3702G>T	NP_001374144.1:n.640-3702G>T
NM_001387216.1:c.640-3702G>T	NP_001374145.1:n.640-3702G>T
NM_001387217.1:c.505-3702G>T	NP_001374146.1:n.505-3702G>T
NM_015307.2:c.928-3702G>T MANE Select	NP_056122.1:n.928-3702G>T