Canonical Allele Identifier: CA2706403632

Gene: ANTXR2

Linked Data

• dbSNP Id: rs2110129627

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072756T>C , CM000666.2:g.80072756T>C	GRCh38
NC_000004.11:g.80993910T>C , CM000666.1:g.80993910T>C	GRCh37
NC_000004.10:g.81212934T>C	NCBI36
NG_015987.1:g.5568A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-196A>G MANE Select	ENSP00000385575.2:n.-196A>G
ENST00000679571.1:c.-127A>G	ENSP00000506307.1:n.-127A>G
ENST00000681115.1:c.-196A>G	ENSP00000505618.1:n.-196A>G
ENST00000681710.1:c.-127A>G	ENSP00000505865.1:n.-127A>G
ENST00000403729.6:c.-196A>G	ENSP00000385575.2:n.-196A>G
ENST00000404191.5:c.-80+639A>G	ENSP00000384028.1:n.-80+639A>G
ENST00000506286.1:n.630-1102A>G
ENST00000514959.1:n.248+6597A>G
NM_001145794.1:c.-196A>G	NP_001139266.1:n.-196A>G
NM_001286780.1:c.-80+639A>G	NP_001273709.1:n.-80+639A>G
NM_001286781.1:c.-127A>G	NP_001273710.1:n.-127A>G
NM_058172.5:c.-196A>G	NP_477520.2:n.-196A>G
XM_011531587.1:c.-80+639A>G	XP_011529889.1:n.-80+639A>G
XM_011531587.3:c.-80+639A>G	XP_011529889.1:n.-80+639A>G
NM_058172.6:c.-196A>G MANE Select	NP_477520.2:n.-196A>G
NM_001286780.2:c.-80+639A>G	NP_001273709.1:n.-80+639A>G
NM_001286781.2:c.-127A>G	NP_001273710.1:n.-127A>G
NM_001145794.2:c.-196A>G	NP_001139266.1:n.-196A>G