Canonical Allele Identifier: CA2036978860
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429970T= , CM000674.2:g.53429970T= GRCh38
NC_000012.11:g.53823754T= , CM000674.1:g.53823754T= GRCh37
NC_000012.10:g.52110021T= NCBI36
NG_015981.1:g.11116T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1280T= MANE Select ENSP00000257863.3:p.Leu427=
ENST00000257863.8:c.1280T= ENSP00000257863.3:p.Leu427=
ENST00000379791.7:c.1140+345T= ENSP00000369117.3:n.1140+345T=
ENST00000550311.5:c.1280T= ENSP00000446661.1:p.Leu427=
ENST00000550839.1:c.371T= ENSP00000455338.1:p.Leu124=
ENST00000552233.5:n.868T=
NM_001164690.1:c.1280T= NP_001158162.1:p.Leu427=
NM_001164691.1:c.1140+345T= NP_001158163.1:n.1140+345T=
NM_020547.2:c.1280T= NP_065434.1:p.Leu427=
XM_011538173.1:c.1340T= XP_011536475.1:p.Leu447=
XM_011538174.1:c.1337T= XP_011536476.1:p.Leu446=
XM_011538175.1:c.1322T= XP_011536477.1:p.Leu441=
XM_011538176.1:c.1283T= XP_011536478.1:p.Leu428=
XM_011538177.1:c.1262T= XP_011536479.1:p.Leu421=
XM_011538178.1:c.1121T= XP_011536480.1:p.Leu374=
XM_011538179.1:c.1200+345T= XP_011536481.1:n.1200+345T=
XM_011538180.1:c.1007T= XP_011536482.1:p.Leu336=
XM_011538181.1:c.1004T= XP_011536483.1:p.Leu335=
XM_011538182.1:c.929T= XP_011536484.1:p.Leu310=
XM_011538183.1:c.1201-176T= XP_011536485.1:n.1201-176T=
XM_011538184.1:c.1220+325T= XP_011536486.1:n.1220+325T=
XM_011538185.1:c.856-1207T= XP_011536487.1:n.856-1207T=
XM_011538186.1:c.455T= XP_011536488.1:p.Leu152=
NM_001164690.2:c.1280T= NP_001158162.1:p.Leu427=
NM_001164691.2:c.1140+345T= NP_001158163.1:n.1140+345T=
NM_020547.3:c.1280T= MANE Select NP_065434.1:p.Leu427=
XM_011538183.2:c.1201-176T= XP_011536485.1:n.1201-176T=
XM_011538184.2:c.1220+325T= XP_011536486.1:n.1220+325T=
XM_011538186.3:c.455T= XP_011536488.1:p.Leu152=
XM_017019179.2:c.1340T= XP_016874668.1:p.Leu447=
XM_024448938.1:c.1143+345T= XP_024304706.1:n.1143+345T=
XR_002957309.1:n.1248T=
XR_002957310.1:n.1109-176T=
XR_002957311.1:n.1248T=
XR_002957312.1:n.1108+345T=