Canonical Allele Identifier: CA2036978775
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429861C= , CM000674.2:g.53429861C= GRCh38
NC_000012.11:g.53823645C= , CM000674.1:g.53823645C= GRCh37
NC_000012.10:g.52109912C= NCBI36
NG_015981.1:g.11007C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1171C= MANE Select ENSP00000257863.3:p.Leu391=
ENST00000257863.8:c.1171C= ENSP00000257863.3:p.Leu391=
ENST00000379791.7:c.1140+236C= ENSP00000369117.3:n.1140+236C=
ENST00000550311.5:c.1171C= ENSP00000446661.1:p.Leu391=
ENST00000550839.1:c.262C= ENSP00000455338.1:p.Leu88=
ENST00000552233.5:n.759C=
NM_001164690.1:c.1171C= NP_001158162.1:p.Leu391=
NM_001164691.1:c.1140+236C= NP_001158163.1:n.1140+236C=
NM_020547.2:c.1171C= NP_065434.1:p.Leu391=
XM_011538173.1:c.1231C= XP_011536475.1:p.Leu411=
XM_011538174.1:c.1228C= XP_011536476.1:p.Leu410=
XM_011538175.1:c.1213C= XP_011536477.1:p.Leu405=
XM_011538176.1:c.1174C= XP_011536478.1:p.Leu392=
XM_011538177.1:c.1153C= XP_011536479.1:p.Leu385=
XM_011538178.1:c.1012C= XP_011536480.1:p.Leu338=
XM_011538179.1:c.1200+236C= XP_011536481.1:n.1200+236C=
XM_011538180.1:c.898C= XP_011536482.1:p.Leu300=
XM_011538181.1:c.895C= XP_011536483.1:p.Leu299=
XM_011538182.1:c.820C= XP_011536484.1:p.Leu274=
XM_011538183.1:c.1200+236C= XP_011536485.1:n.1200+236C=
XM_011538184.1:c.1220+216C= XP_011536486.1:n.1220+216C=
XM_011538185.1:c.856-1316C= XP_011536487.1:n.856-1316C=
XM_011538186.1:c.346C= XP_011536488.1:p.Leu116=
NM_001164690.2:c.1171C= NP_001158162.1:p.Leu391=
NM_001164691.2:c.1140+236C= NP_001158163.1:n.1140+236C=
NM_020547.3:c.1171C= MANE Select NP_065434.1:p.Leu391=
XM_011538183.2:c.1200+236C= XP_011536485.1:n.1200+236C=
XM_011538184.2:c.1220+216C= XP_011536486.1:n.1220+216C=
XM_011538186.3:c.346C= XP_011536488.1:p.Leu116=
XM_017019179.2:c.1231C= XP_016874668.1:p.Leu411=
XM_024448938.1:c.1143+236C= XP_024304706.1:n.1143+236C=
XR_002957309.1:n.1139C=
XR_002957310.1:n.1108+236C=
XR_002957311.1:n.1139C=
XR_002957312.1:n.1108+236C=