Canonical Allele Identifier: CA14176450

Gene: ENTREP2

Linked Data

• dbSNP Id: rs2636061
• gnomAD v2: 15-29424755-A-G
• gnomAD v3: 15-29132552-A-G
• gnomAD v4: 15-29132552-A-G
• MyVariant Identifiers: chr15:g.29424755A>G (hg19) ; chr15:g.29132552A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132552A>G , CM000677.2:g.29132552A>G	GRCh38
NC_000015.9:g.29424755A>G , CM000677.1:g.29424755A>G	GRCh37
NC_000015.8:g.27212047A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261275.5:c.928-3688T>C MANE Select	ENSP00000261275.4:n.928-3688T>C
ENST00000261275.4:c.928-3688T>C	ENSP00000261275.4:n.928-3688T>C
ENST00000560021.1:n.664-3688T>C
NM_015307.1:c.928-3688T>C	NP_056122.1:n.928-3688T>C
XM_011521407.1:c.1039-3688T>C	XP_011519709.1:n.1039-3688T>C
XM_011521407.2:c.1039-3688T>C	XP_011519709.1:n.1039-3688T>C
NM_001387214.1:c.793-3688T>C	NP_001374143.1:n.793-3688T>C
NM_001387215.1:c.640-3688T>C	NP_001374144.1:n.640-3688T>C
NM_001387216.1:c.640-3688T>C	NP_001374145.1:n.640-3688T>C
NM_001387217.1:c.505-3688T>C	NP_001374146.1:n.505-3688T>C
NM_015307.2:c.928-3688T>C MANE Select	NP_056122.1:n.928-3688T>C