Canonical Allele Identifier: CA2036978760
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429842G= , CM000674.2:g.53429842G= GRCh38
NC_000012.11:g.53823626G= , CM000674.1:g.53823626G= GRCh37
NC_000012.10:g.52109893G= NCBI36
NG_015981.1:g.10988G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1152G= MANE Select ENSP00000257863.3:p.Gln384=
ENST00000257863.8:c.1152G= ENSP00000257863.3:p.Gln384=
ENST00000379791.7:c.1140+217G= ENSP00000369117.3:n.1140+217G=
ENST00000550311.5:c.1152G= ENSP00000446661.1:p.Gln384=
ENST00000550839.1:c.243G= ENSP00000455338.1:p.Gln81=
ENST00000552233.5:n.740G=
NM_001164690.1:c.1152G= NP_001158162.1:p.Gln384=
NM_001164691.1:c.1140+217G= NP_001158163.1:n.1140+217G=
NM_020547.2:c.1152G= NP_065434.1:p.Gln384=
XM_011538173.1:c.1212G= XP_011536475.1:p.Gln404=
XM_011538174.1:c.1209G= XP_011536476.1:p.Gln403=
XM_011538175.1:c.1194G= XP_011536477.1:p.Gln398=
XM_011538176.1:c.1155G= XP_011536478.1:p.Gln385=
XM_011538177.1:c.1134G= XP_011536479.1:p.Gln378=
XM_011538178.1:c.993G= XP_011536480.1:p.Gln331=
XM_011538179.1:c.1200+217G= XP_011536481.1:n.1200+217G=
XM_011538180.1:c.879G= XP_011536482.1:p.Gln293=
XM_011538181.1:c.876G= XP_011536483.1:p.Gln292=
XM_011538182.1:c.801G= XP_011536484.1:p.Gln267=
XM_011538183.1:c.1200+217G= XP_011536485.1:n.1200+217G=
XM_011538184.1:c.1220+197G= XP_011536486.1:n.1220+197G=
XM_011538185.1:c.856-1335G= XP_011536487.1:n.856-1335G=
XM_011538186.1:c.327G= XP_011536488.1:p.Gln109=
NM_001164690.2:c.1152G= NP_001158162.1:p.Gln384=
NM_001164691.2:c.1140+217G= NP_001158163.1:n.1140+217G=
NM_020547.3:c.1152G= MANE Select NP_065434.1:p.Gln384=
XM_011538183.2:c.1200+217G= XP_011536485.1:n.1200+217G=
XM_011538184.2:c.1220+197G= XP_011536486.1:n.1220+197G=
XM_011538186.3:c.327G= XP_011536488.1:p.Gln109=
XM_017019179.2:c.1212G= XP_016874668.1:p.Gln404=
XM_024448938.1:c.1143+217G= XP_024304706.1:n.1143+217G=
XR_002957309.1:n.1120G=
XR_002957310.1:n.1108+217G=
XR_002957311.1:n.1120G=
XR_002957312.1:n.1108+217G=