Canonical Allele Identifier: CA2036978770
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429852G= , CM000674.2:g.53429852G= GRCh38
NC_000012.11:g.53823636G= , CM000674.1:g.53823636G= GRCh37
NC_000012.10:g.52109903G= NCBI36
NG_015981.1:g.10998G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1162G= MANE Select ENSP00000257863.3:p.Ala388=
ENST00000257863.8:c.1162G= ENSP00000257863.3:p.Ala388=
ENST00000379791.7:c.1140+227G= ENSP00000369117.3:n.1140+227G=
ENST00000550311.5:c.1162G= ENSP00000446661.1:p.Ala388=
ENST00000550839.1:c.253G= ENSP00000455338.1:p.Ala85=
ENST00000552233.5:n.750G=
NM_001164690.1:c.1162G= NP_001158162.1:p.Ala388=
NM_001164691.1:c.1140+227G= NP_001158163.1:n.1140+227G=
NM_020547.2:c.1162G= NP_065434.1:p.Ala388=
XM_011538173.1:c.1222G= XP_011536475.1:p.Ala408=
XM_011538174.1:c.1219G= XP_011536476.1:p.Ala407=
XM_011538175.1:c.1204G= XP_011536477.1:p.Ala402=
XM_011538176.1:c.1165G= XP_011536478.1:p.Ala389=
XM_011538177.1:c.1144G= XP_011536479.1:p.Ala382=
XM_011538178.1:c.1003G= XP_011536480.1:p.Ala335=
XM_011538179.1:c.1200+227G= XP_011536481.1:n.1200+227G=
XM_011538180.1:c.889G= XP_011536482.1:p.Ala297=
XM_011538181.1:c.886G= XP_011536483.1:p.Ala296=
XM_011538182.1:c.811G= XP_011536484.1:p.Ala271=
XM_011538183.1:c.1200+227G= XP_011536485.1:n.1200+227G=
XM_011538184.1:c.1220+207G= XP_011536486.1:n.1220+207G=
XM_011538185.1:c.856-1325G= XP_011536487.1:n.856-1325G=
XM_011538186.1:c.337G= XP_011536488.1:p.Ala113=
NM_001164690.2:c.1162G= NP_001158162.1:p.Ala388=
NM_001164691.2:c.1140+227G= NP_001158163.1:n.1140+227G=
NM_020547.3:c.1162G= MANE Select NP_065434.1:p.Ala388=
XM_011538183.2:c.1200+227G= XP_011536485.1:n.1200+227G=
XM_011538184.2:c.1220+207G= XP_011536486.1:n.1220+207G=
XM_011538186.3:c.337G= XP_011536488.1:p.Ala113=
XM_017019179.2:c.1222G= XP_016874668.1:p.Ala408=
XM_024448938.1:c.1143+227G= XP_024304706.1:n.1143+227G=
XR_002957309.1:n.1130G=
XR_002957310.1:n.1108+227G=
XR_002957311.1:n.1130G=
XR_002957312.1:n.1108+227G=