Canonical Allele Identifier: CA373836350
Gene: AUH HGNC NCBI

Linked Data

dbSNP Id: rs1179657132

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91361712C>G , CM000671.2:g.91361712C>G GRCh38
NC_000009.11:g.94123994C>G , CM000671.1:g.94123994C>G GRCh37
NC_000009.10:g.93163815C>G NCBI36
NG_008017.1:g.5213G>C , LRG_449:g.5213G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375731.9:c.178G>C MANE Select ENSP00000364883.5:p.Gly60Arg
ENST00000303617.5:c.178G>C ENSP00000307334.5:p.Gly60Arg
ENST00000375731.8:c.178G>C ENSP00000364883.4:p.Gly60Arg
ENST00000478465.5:n.176G>C
NM_001306190.1:c.178G>C NP_001293119.1:p.Gly60Arg
NM_001698.2:c.178G>C , LRG_449t1:c.178G>C NP_001689.1:p.Gly60Arg
XM_005252066.2:c.178G>C XP_005252123.1:p.Gly60Arg
XM_005252067.3:c.178G>C XP_005252124.1:p.Gly60Arg
XM_005252069.3:c.178G>C XP_005252126.1:p.Gly60Arg
XM_005252072.1:c.178G>C XP_005252129.1:p.Gly60Arg
XM_006717150.2:c.178G>C XP_006717213.1:p.Gly60Arg
XM_011518800.1:c.178G>C XP_011517102.1:p.Gly60Arg
XM_011518802.1:c.-220G>C XP_011517104.1:n.-220G>C
XM_011518803.1:c.178G>C XP_011517105.1:p.Gly60Arg
XM_011518804.1:c.178G>C XP_011517106.1:p.Gly60Arg
XR_929814.1:n.228G>C
NM_001351431.1:c.-220G>C NP_001338360.1:n.-220G>C
NM_001351432.1:c.-312G>C NP_001338361.1:n.-312G>C
NM_001351433.1:c.-220G>C NP_001338362.1:n.-220G>C
XM_005252066.3:c.178G>C XP_005252123.1:p.Gly60Arg
XM_005252067.4:c.178G>C XP_005252124.1:p.Gly60Arg
XM_005252069.4:c.178G>C XP_005252126.1:p.Gly60Arg
XM_005252072.2:c.178G>C XP_005252129.1:p.Gly60Arg
XM_006717150.3:c.178G>C XP_006717213.1:p.Gly60Arg
XM_011518800.3:c.178G>C XP_011517102.1:p.Gly60Arg
XM_011518803.2:c.178G>C XP_011517105.1:p.Gly60Arg
XM_017014849.1:c.178G>C XP_016870338.1:p.Gly60Arg
XR_001746328.2:n.231G>C
XR_001746329.2:n.213G>C
NM_001698.3:c.178G>C MANE Select NP_001689.1:p.Gly60Arg
NM_001306190.2:c.178G>C NP_001293119.1:p.Gly60Arg
NM_001351431.2:c.-220G>C NP_001338360.1:n.-220G>C
NM_001351432.2:c.-312G>C NP_001338361.1:n.-312G>C
NM_001351433.2:c.-220G>C NP_001338362.1:n.-220G>C