Canonical Allele Identifier: CA267968454

Gene: ENTREP2

Linked Data

• dbSNP Id: rs575111996
• gnomAD v3: 15-29132572-G-T
• gnomAD v4: 15-29132572-G-T
• MyVariant Identifiers: chr15:g.29424775G>T (hg19) ; chr15:g.29132572G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132572G>T , CM000677.2:g.29132572G>T	GRCh38
NC_000015.9:g.29424775G>T , CM000677.1:g.29424775G>T	GRCh37
NC_000015.8:g.27212067G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261275.5:c.928-3708C>A MANE Select	ENSP00000261275.4:n.928-3708C>A
ENST00000261275.4:c.928-3708C>A	ENSP00000261275.4:n.928-3708C>A
ENST00000560021.1:n.664-3708C>A
NM_015307.1:c.928-3708C>A	NP_056122.1:n.928-3708C>A
XM_011521407.1:c.1039-3708C>A	XP_011519709.1:n.1039-3708C>A
XM_011521407.2:c.1039-3708C>A	XP_011519709.1:n.1039-3708C>A
NM_001387214.1:c.793-3708C>A	NP_001374143.1:n.793-3708C>A
NM_001387215.1:c.640-3708C>A	NP_001374144.1:n.640-3708C>A
NM_001387216.1:c.640-3708C>A	NP_001374145.1:n.640-3708C>A
NM_001387217.1:c.505-3708C>A	NP_001374146.1:n.505-3708C>A
NM_015307.2:c.928-3708C>A MANE Select	NP_056122.1:n.928-3708C>A