Canonical Allele Identifier: CA2619052897
Gene: AMHR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429750_53429751dup , CM000674.2:g.53429750_53429751dup GRCh38
NC_000012.11:g.53823534_53823535dup , CM000674.1:g.53823534_53823535dup GRCh37
NC_000012.10:g.52109801_52109802dup NCBI36
NG_015981.1:g.10896_10897dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1141-81_1141-80dup MANE Select ENSP00000257863.3:n.1141-81_1141-80dup
ENST00000257863.8:c.1141-81_1141-80dup ENSP00000257863.3:n.1141-81_1141-80dup
ENST00000379791.7:c.1140+125_1140+126dup ENSP00000369117.3:n.1140+125_1140+126dup
ENST00000550311.5:c.1141-81_1141-80dup ENSP00000446661.1:n.1141-81_1141-80dup
ENST00000550839.1:c.232-81_232-80dup ENSP00000455338.1:n.232-81_232-80dup
ENST00000552233.5:n.648_649dup
NM_001164690.1:c.1141-81_1141-80dup NP_001158162.1:n.1141-81_1141-80dup
NM_001164691.1:c.1140+125_1140+126dup NP_001158163.1:n.1140+125_1140+126dup
NM_020547.2:c.1141-81_1141-80dup NP_065434.1:n.1141-81_1141-80dup
XM_011538173.1:c.1201-81_1201-80dup XP_011536475.1:n.1201-81_1201-80dup
XM_011538174.1:c.1198-81_1198-80dup XP_011536476.1:n.1198-81_1198-80dup
XM_011538175.1:c.1183-81_1183-80dup XP_011536477.1:n.1183-81_1183-80dup
XM_011538176.1:c.1144-81_1144-80dup XP_011536478.1:n.1144-81_1144-80dup
XM_011538177.1:c.1123-81_1123-80dup XP_011536479.1:n.1123-81_1123-80dup
XM_011538178.1:c.982-81_982-80dup XP_011536480.1:n.982-81_982-80dup
XM_011538179.1:c.1200+125_1200+126dup XP_011536481.1:n.1200+125_1200+126dup
XM_011538180.1:c.868-81_868-80dup XP_011536482.1:n.868-81_868-80dup
XM_011538181.1:c.865-81_865-80dup XP_011536483.1:n.865-81_865-80dup
XM_011538182.1:c.790-81_790-80dup XP_011536484.1:n.790-81_790-80dup
XM_011538183.1:c.1200+125_1200+126dup XP_011536485.1:n.1200+125_1200+126dup
XM_011538184.1:c.1220+105_1220+106dup XP_011536486.1:n.1220+105_1220+106dup
XM_011538185.1:c.856-1427_856-1426dup XP_011536487.1:n.856-1427_856-1426dup
XM_011538186.1:c.316-81_316-80dup XP_011536488.1:n.316-81_316-80dup
NM_001164690.2:c.1141-81_1141-80dup NP_001158162.1:n.1141-81_1141-80dup
NM_001164691.2:c.1140+125_1140+126dup NP_001158163.1:n.1140+125_1140+126dup
NM_020547.3:c.1141-81_1141-80dup MANE Select NP_065434.1:n.1141-81_1141-80dup
XM_011538183.2:c.1200+125_1200+126dup XP_011536485.1:n.1200+125_1200+126dup
XM_011538184.2:c.1220+105_1220+106dup XP_011536486.1:n.1220+105_1220+106dup
XM_011538186.3:c.316-81_316-80dup XP_011536488.1:n.316-81_316-80dup
XM_017019179.2:c.1201-81_1201-80dup XP_016874668.1:n.1201-81_1201-80dup
XM_024448938.1:c.1143+125_1143+126dup XP_024304706.1:n.1143+125_1143+126dup
XR_002957309.1:n.1109-81_1109-80dup
XR_002957310.1:n.1108+125_1108+126dup
XR_002957311.1:n.1109-81_1109-80dup
XR_002957312.1:n.1108+125_1108+126dup