Canonical Allele Identifier: CA2036978788
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429886A= , CM000674.2:g.53429886A= GRCh38
NC_000012.11:g.53823670A= , CM000674.1:g.53823670A= GRCh37
NC_000012.10:g.52109937A= NCBI36
NG_015981.1:g.11032A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1196A= MANE Select ENSP00000257863.3:p.Gln399=
ENST00000257863.8:c.1196A= ENSP00000257863.3:p.Gln399=
ENST00000379791.7:c.1140+261A= ENSP00000369117.3:n.1140+261A=
ENST00000550311.5:c.1196A= ENSP00000446661.1:p.Gln399=
ENST00000550839.1:c.287A= ENSP00000455338.1:p.Gln96=
ENST00000552233.5:n.784A=
NM_001164690.1:c.1196A= NP_001158162.1:p.Gln399=
NM_001164691.1:c.1140+261A= NP_001158163.1:n.1140+261A=
NM_020547.2:c.1196A= NP_065434.1:p.Gln399=
XM_011538173.1:c.1256A= XP_011536475.1:p.Gln419=
XM_011538174.1:c.1253A= XP_011536476.1:p.Gln418=
XM_011538175.1:c.1238A= XP_011536477.1:p.Gln413=
XM_011538176.1:c.1199A= XP_011536478.1:p.Gln400=
XM_011538177.1:c.1178A= XP_011536479.1:p.Gln393=
XM_011538178.1:c.1037A= XP_011536480.1:p.Gln346=
XM_011538179.1:c.1200+261A= XP_011536481.1:n.1200+261A=
XM_011538180.1:c.923A= XP_011536482.1:p.Gln308=
XM_011538181.1:c.920A= XP_011536483.1:p.Gln307=
XM_011538182.1:c.845A= XP_011536484.1:p.Gln282=
XM_011538183.1:c.1201-260A= XP_011536485.1:n.1201-260A=
XM_011538184.1:c.1220+241A= XP_011536486.1:n.1220+241A=
XM_011538185.1:c.856-1291A= XP_011536487.1:n.856-1291A=
XM_011538186.1:c.371A= XP_011536488.1:p.Gln124=
NM_001164690.2:c.1196A= NP_001158162.1:p.Gln399=
NM_001164691.2:c.1140+261A= NP_001158163.1:n.1140+261A=
NM_020547.3:c.1196A= MANE Select NP_065434.1:p.Gln399=
XM_011538183.2:c.1201-260A= XP_011536485.1:n.1201-260A=
XM_011538184.2:c.1220+241A= XP_011536486.1:n.1220+241A=
XM_011538186.3:c.371A= XP_011536488.1:p.Gln124=
XM_017019179.2:c.1256A= XP_016874668.1:p.Gln419=
XM_024448938.1:c.1143+261A= XP_024304706.1:n.1143+261A=
XR_002957309.1:n.1164A=
XR_002957310.1:n.1109-260A=
XR_002957311.1:n.1164A=
XR_002957312.1:n.1108+261A=