Canonical Allele Identifier: CA2671171696

Gene: ANTXR2

Linked Data

• gnomAD v4: 4-80072767-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072767G>C , CM000666.2:g.80072767G>C	GRCh38
NC_000004.11:g.80993921G>C , CM000666.1:g.80993921G>C	GRCh37
NC_000004.10:g.81212945G>C	NCBI36
NG_015987.1:g.5557C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-207C>G MANE Select	ENSP00000385575.2:n.-207C>G
ENST00000679571.1:c.-138C>G	ENSP00000506307.1:n.-138C>G
ENST00000681115.1:c.-207C>G	ENSP00000505618.1:n.-207C>G
ENST00000681710.1:c.-138C>G	ENSP00000505865.1:n.-138C>G
ENST00000403729.6:c.-207C>G	ENSP00000385575.2:n.-207C>G
ENST00000404191.5:c.-80+628C>G	ENSP00000384028.1:n.-80+628C>G
ENST00000506286.1:n.630-1113C>G
ENST00000514959.1:n.248+6586C>G
NM_001145794.1:c.-207C>G	NP_001139266.1:n.-207C>G
NM_001286780.1:c.-80+628C>G	NP_001273709.1:n.-80+628C>G
NM_001286781.1:c.-138C>G	NP_001273710.1:n.-138C>G
NM_058172.5:c.-207C>G	NP_477520.2:n.-207C>G
XM_011531587.1:c.-80+628C>G	XP_011529889.1:n.-80+628C>G
XM_011531587.3:c.-80+628C>G	XP_011529889.1:n.-80+628C>G
NM_058172.6:c.-207C>G MANE Select	NP_477520.2:n.-207C>G
NM_001286780.2:c.-80+628C>G	NP_001273709.1:n.-80+628C>G
NM_001286781.2:c.-138C>G	NP_001273710.1:n.-138C>G
NM_001145794.2:c.-207C>G	NP_001139266.1:n.-207C>G